heparin sodium

Generic: heparin sodium

Labeler: be pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name heparin sodium
Generic Name heparin sodium
Labeler be pharmaceuticals inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS SUBCUTANEOUS
Active Ingredients

heparin sodium 2000 [USP'U]/2mL

Manufacturer
BE Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 71839-117
Product ID 71839-117_4d2cbee1-f461-45a1-bf5f-c8dd4ef8501b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214804
Listing Expiration 2026-12-31
Marketing Start 2020-12-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71839117
Hyphenated Format 71839-117

Supplemental Identifiers

RxCUI
1658647
UPC
0371839117017
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 ANDA214804 (source: ndc)
Routes
INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 2000 [USP'U]/2mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 CARTON (71839-117-25) / 2 mL in 1 VIAL, SINGLE-DOSE (71839-117-01)
source: ndc

Packages (1)

71839-117-25 25 VIAL, SINGLE-DOSE in 1 CARTON (71839-117-25) / 2 mL in 1 VIAL, SINGLE-DOSE (71839-117-01)

Ingredients (1)

heparin sodium (2000 [USP'U]/2mL)

Linked Drug Pages (1)

Heparin Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "4d2cbee1-f461-45a1-bf5f-c8dd4ef8501b", "openfda": {"upc": ["0371839117017"], "unii": ["ZZ45AB24CA"], "rxcui": ["1658647"], "spl_set_id": ["295ea9c6-d08c-40f0-a908-de0fdac44644"], "manufacturer_name": ["BE Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (71839-117-25)  / 2 mL in 1 VIAL, SINGLE-DOSE (71839-117-01)", "package_ndc": "71839-117-25", "marketing_start_date": "20201229"}], "brand_name": "Heparin Sodium", "product_id": "71839-117_4d2cbee1-f461-45a1-bf5f-c8dd4ef8501b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "71839-117", "generic_name": "Heparin Sodium", "labeler_name": "BE Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "2000 [USP'U]/2mL"}], "application_number": "ANDA214804", "marketing_category": "ANDA", "marketing_start_date": "20201229", "listing_expiration_date": "20261231"}