heparin sodium

Generic: heparin sodium

Labeler: mckesson corporation dba sky packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name heparin sodium
Generic Name heparin sodium
Labeler mckesson corporation dba sky packaging
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS SUBCUTANEOUS
Active Ingredients

heparin sodium 1000 [USP'U]/mL

Manufacturer
McKesson Corporation dba SKY Packaging

Identifiers & Regulatory

Product NDC 63739-931
Product ID 63739-931_2c31ae6a-f9c6-fb65-e063-6294a90af0e1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202957
Listing Expiration 2026-12-31
Marketing Start 2014-06-12

Pharmacologic Class

Classes
anti-coagulant [epc] heparin [cs] unfractionated heparin [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63739931
Hyphenated Format 63739-931

Supplemental Identifiers

RxCUI
1361226 1361574 1361615 1362831 1658647
UPC
0363739986251 0363739975279 0363739964259 0363739942158 0363739953253 0363739900264 0363739920255
UNII
ZZ45AB24CA

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name heparin sodium (source: ndc)
Generic Name heparin sodium (source: ndc)
Application Number ANDA202957 (source: ndc)
Routes
INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 1000 [USP'U]/mL
source: ndc
Packaging
  • 16 HOW SUPPLIED/STORAGE AND HANDLING Heparin sodium injection, USP (porcine), preservative free, is available as follows: NDC Number Concentration Vial Fill Volume Vial Type Pack Size 63739-900-26 1,000 USP Heparin Units/mL 2 mL Single-Dose Vial Carton of 25 vials Use only if solution is clear and seal intact. Do not use if solution is discolored or contains a precipitate. This container closure is not made with natural rubber latex. Discard unused portion. Heparin Sodium Injection, USP (porcine) contains benzyl alcohol and is available as follows: NDC Number Concentration Vial Fill Volume Vial Type Pack Size 63739-901-28 5,000 USP Heparin Units/mL 10 mL Multiple-Dose Vial Carton of 25 vials Use only if solution is clear and seal intact. Do not use if solution is discolored or contains a precipitate. This container closure is not made with natural rubber latex. Heparin Sodium Injection, USP (porcine) contains parabens and is available as follows: NDC Number Concentration Vial Fill Volume Vial Type Pack Size 63739-920-25 1,000 USP Heparin Units/mL 1 mL Multiple-Dose Vial Carton of 25 vials 63739-931-28 1,000 USP Heparin Units/mL 10 mL Multiple-Dose Vial Carton of 25 vials 63739-942-29 1,000 USP Heparin Units/mL 30 mL Multiple-Dose Vial Carton of 25 vials 63739-953-25 5,000 USP Heparin Units/mL 1 mL Multiple-Dose Vial Carton of 25 vials 63739-964-25 10,000 USP Heparin Units/mL 1 mL Multiple-Dose Vial Carton of 25 vials 63739-975-27 10,000 USP Heparin Units/mL 5 mL Multiple-Dose Vial Carton of 25 vials 63739-986-25 20,000 USP Heparin Units/mL 1 mL Multiple-Dose Vial Carton of 25 vials Use only if solution is clear and seal intact. Do not use if solution is discolored or contains a precipitate. This container closure is not made with natural rubber latex. STORAGE: Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 1,000 USP Units/mL - 1 mL Container Label NDC 63739-920-11 Rx only HEPARIN SODIUM INJECTION, USP 1,000 USP Units/mL For IV or SC use Multiple Dose Vial 1 mL NOT FOR LOCK FLUSH heparin-fig1
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 1,000 USP Units/mL - 1 mL Container-Carton [25 Multiple Dose Vials] NDC 63739-920-25 Rx only HEPARIN SODIUM INJECTION, USP 1,000 USP Units/mL 1 mL NOT FOR LOCK FLUSH For Intravenous or Subcutaneous use 25 Multiple-Dose Vials Derived from Porcine Intestinal Mucosa heparin-fig2
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10,000 USP Units/10 mL (1,000 USP Units/mL) - 10 mL Container Label NDC 63739-931-14 Rx only HEPARIN SODIUM INJECTION, USP 10,000 USP Units/10 mL (1,000 USP Units/mL) For IV or SC use 10 mL Multiple Dose Vial NOT FOR LOCK FLUSH heparin-fig3
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10,000 USP Units/10 mL (1,000 USP Units/mL) - 10 mL Container-Carton [25 Multiple Dose Vials] NDC 63739-931-28 Rx only HEPARIN SODIUM INJECTION, USP 10,000 USP Units/10 mL (1,000 USP Units/mL) 10 mL NOT FOR LOCK FLUSH For Intravenous or Subcutaneous use 25 Multiple-Dose Vials Derived from Porcine Intestinal Mucosa heparin-fig4
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 30,000 USP Units/30 mL (1,000 USP Units/mL) - 30 mL Container Label NDC 63739-942-15 Rx only HEPARIN SODIUM INJECTION, USP 30,000 USP Units/30 mL (1,000 USP Units/mL) For IV or SC use Multiple Dose Vial 30 mL NOT FOR LOCK FLUSH heparin-fig5
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 30,000 USP Units/30 mL (1,000 USP Units/mL) - 30 mL Container-Carton [25 Multiple Dose Vials] NDC 63739-942-29 Rx only HEPARIN SODIUM INJECTION, USP 30,000 USP Units/30 mL (1,000 USP Units/mL) 30 mL NOT FOR LOCK FLUSH For Intravenous or Subcutaneous use 25 Multiple-Dose Vials Derived from Porcine Intestinal Mucosa heparin-fig6
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 5,000 USP Units/mL - 1 mL Container Label NDC 63739-953-11 Rx only HEPARIN SODIUM INJECTION, USP 5,000 USP Units/mL For IV or SC use Multiple Dose Vial 1 mL NOT FOR LOCK FLUSH heparin-fig7
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 5,000 USP Units/mL - 1 mL Container-Carton [25 Multiple Dose Vials] NDC 63739-953-25 Rx only HEPARIN SODIUM INJECTION, USP 5,000 USP Units/mL 1 mL NOT FOR LOCK FLUSH For Intravenous or Subcutaneous use 25 Multiple-Dose Vials Derived from Porcine Intestinal Mucosa heparin-fig8
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10,000 USP Units/mL - 1 mL Container Label NDC 63739-964-11 Rx only HEPARIN SODIUM INJECTION, USP 10,000 USP Units/mL For IV or SC use Multiple Dose Vial 1 mL NOT FOR LOCK FLUSH heparin-fig9
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10,000 USP Units/mL - 1 mL Container-Carton [25 Multiple Dose Vials] NDC 63739-964-25 Rx only HEPARIN SODIUM INJECTION, USP 10,000 USP Units/mL 1 mL NOT FOR LOCK FLUSH For Intravenous or Subcutaneous use 25 Multiple-Dose Vials Derived from Porcine Intestinal Mucosa heparin-fig10
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 50,000 USP Units/5 mL (10,000 USP Units/mL) - 5 mL Container Label NDC 63739-975-13 Rx only HEPARIN SODIUM INJECTION, USP 50,000 USP Units/5 mL (10,000 USP Units/mL) For IV or SC use Multiple Dose Vial 5 mL NOT FOR LOCK FLUSH heparin-fig11
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 50,000 USP Units/5 mL (10,000 USP Units/mL) - 5 mL Container-Carton [25 Multiple Dose Vials] NDC 63739-975-27 Rx only HEPARIN SODIUM INJECTION, USP 50,000 USP Units/5 mL (10,000 USP Units/mL) 5 mL NOT FOR LOCK FLUSH For Intravenous or Subcutaneous use 25 Multiple-Dose Vials Derived from Porcine Intestinal Mucosa heparin-fig12
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 20,000 USP Units/mL - 1 mL Container Label NDC 63739-986-11 Rx only HEPARIN SODIUM INJECTION, USP 20,000 USP Units/mL For IV or SC use Multiple Dose Vial 1 mL NOT FOR LOCK FLUSH heparin-fig13
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 20,000 USP Units/mL - 1 mL Container-Carton [25 Multiple Dose Vials] NDC 63739-986-25 Rx only HEPARIN SODIUM INJECTION, USP 20,000 USP Units/mL 1 mL NOT FOR LOCK FLUSH For Intravenous or Subcutaneous use 25 Multiple-Dose Vials Derived from Porcine Intestinal Mucosa heparin-fig14
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL- 2,000 USP Units/2 mL (1,000 USP Units/mL) - 2 mL Container Label NDC 63739-900-12 Rx only HEPARIN SODIUM INJECTION, USP 2,000 USP Units/2 mL (1,000 USP Units/mL) For IV or SC use Preservative Free Discard unused portion 2 mL Single Dose Vial NOT FOR LOCK FLUSH heparin-fig15
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL- 2,000 USP Units/2 mL (1,000 USP Units/mL) - 2 mL Container-Carton [25 Single Dose Vials] NDC 63739-900-26 Rx only HEPARIN SODIUM INJECTION, USP 2,000 USP Units/2 mL (1,000 USP Units/mL) 2 mL NOT FOR LOCK FLUSH For Intravenous or Subcutaneous use Preservative Free 25 Single-Dose Vials Derived from Porcine Intestinal Mucosa heparin-fig16
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL- 50,000 USP Units/10 mL (5,000 USP Units/mL) - 10 mL Container Label NDC 63739-901-14 Rx only HEPARIN SODIUM INJECTION, USP 50,000 USP Units/10 mL (5,000 USP Units/mL) For IV or SC use Warning: Contains Benzyl Alcohol 10 mL Multiple Dose Vial NOT FOR LOCK FLUSH heparin-fig17
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL- 50,000 USP Units/10 mL (5,000 USP Units/mL) - 10 mL Container-Carton [25 Multiple Dose Vials] NDC 63739-901-28 Rx only HEPARIN SODIUM INJECTION, USP 50,000 USP Units/10 mL (5,000 USP Units/mL) 10 mL NOT FOR LOCK FLUSH Warning: Contains Benzyl Alcohol For Intravenous or Subcutaneous use 25 Multiple-Dose Vials Derived from Porcine Intestinal Mucosa heparin-fig18
source: label

Packages (0)

No package records.

Ingredients (1)

heparin sodium (1000 [USP'U]/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "2c31ae6a-f9c6-fb65-e063-6294a90af0e1", "openfda": {"upc": ["0363739986251", "0363739975279", "0363739964259", "0363739942158", "0363739953253", "0363739900264", "0363739920255"], "unii": ["ZZ45AB24CA"], "rxcui": ["1361226", "1361574", "1361615", "1362831", "1658647"], "spl_set_id": ["7f05762a-7527-4796-b21e-68277aec379e"], "manufacturer_name": ["McKesson Corporation dba SKY Packaging"], "is_original_packager": [true]}, "finished": true, "packaging": [], "brand_name": "Heparin Sodium", "product_id": "63739-931_2c31ae6a-f9c6-fb65-e063-6294a90af0e1", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "63739-931", "generic_name": "Heparin Sodium", "labeler_name": "McKesson Corporation dba SKY Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "1000 [USP'U]/mL"}], "application_number": "ANDA202957", "marketing_category": "ANDA", "marketing_start_date": "20140612", "listing_expiration_date": "20261231"}