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, SOLUTION
Routes
Active Ingredients
heparin sodium 5000 [USP'U]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
71288-406
Product ID
71288-406_ab9c214d-f2e3-4043-b2da-b6a56a8b0432
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212061
Listing Expiration
2026-12-31
Marketing Start
2020-07-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71288406
Hyphenated Format
71288-406
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
ANDA212061 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5000 [USP'U]/mL
Packaging
- 24 BLISTER PACK in 1 CARTON (71288-406-82) / 1 SYRINGE, GLASS in 1 BLISTER PACK / 1 mL in 1 SYRINGE, GLASS (71288-406-81)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "ab9c214d-f2e3-4043-b2da-b6a56a8b0432", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1798389"], "spl_set_id": ["57f1ec87-8a7d-41da-b8b8-9ecc8601c60f"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BLISTER PACK in 1 CARTON (71288-406-82) / 1 SYRINGE, GLASS in 1 BLISTER PACK / 1 mL in 1 SYRINGE, GLASS (71288-406-81)", "package_ndc": "71288-406-82", "marketing_start_date": "20200715"}], "brand_name": "Heparin Sodium", "product_id": "71288-406_ab9c214d-f2e3-4043-b2da-b6a56a8b0432", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "71288-406", "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": "5000 [USP'U]/mL"}], "application_number": "ANDA212061", "marketing_category": "ANDA", "marketing_start_date": "20200715", "listing_expiration_date": "20261231"}