heparin sodium

Generic: heparin sodium

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

Drug Facts

Product Profile

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

heparin sodium 2000 [USP'U]/2mL

Manufacturer
Meitheal Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 71288-400
Product ID 71288-400_dabdb746-a0fb-4208-ab3c-32e638396713
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211005
Listing Expiration 2026-12-31
Marketing Start 2019-06-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71288400
Hyphenated Format 71288-400

Supplemental Identifiers

RxCUI
1658647
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 ANDA211005 (source: ndc)
Routes
INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 2000 [USP'U]/2mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 CARTON (71288-400-03) / 2 mL in 1 VIAL, SINGLE-DOSE (71288-400-02)
source: ndc

Packages (1)

Ingredients (1)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "dabdb746-a0fb-4208-ab3c-32e638396713", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658647"], "spl_set_id": ["83a59e7d-63e9-4eb8-87f0-52039d6893a5"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (71288-400-03)  / 2 mL in 1 VIAL, SINGLE-DOSE (71288-400-02)", "package_ndc": "71288-400-03", "marketing_start_date": "20190615"}], "brand_name": "Heparin Sodium", "product_id": "71288-400_dabdb746-a0fb-4208-ab3c-32e638396713", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "71288-400", "generic_name": "Heparin Sodium", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "2000 [USP'U]/2mL"}], "application_number": "ANDA211005", "marketing_category": "ANDA", "marketing_start_date": "20190615", "listing_expiration_date": "20261231"}