heparin sodium
Generic: heparin sodium
Labeler: meitheal pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
heparin sodium
Generic Name
heparin sodium
Labeler
meitheal pharmaceuticals inc.
Dosage Form
INJECTION
Routes
Active Ingredients
heparin sodium 2000 [USP'U]/2mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71288400
Hyphenated Format
71288-400
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 2000 [USP'U]/2mL
Packaging
- 25 VIAL, SINGLE-DOSE in 1 CARTON (71288-400-03) / 2 mL in 1 VIAL, SINGLE-DOSE (71288-400-02)
Packages (1)
Ingredients (1)
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"}