enoxaparin sodium
Generic: enoxaparin sodium
Labeler: be pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
enoxaparin sodium
Generic Name
enoxaparin sodium
Labeler
be pharmaceuticals inc.
Dosage Form
INJECTION
Routes
Active Ingredients
enoxaparin sodium 80 mg/.8mL
Manufacturer
Identifiers & Regulatory
Product NDC
71839-112
Product ID
71839-112_5db5abf2-d207-4e03-a5cc-8e31f2fa20c0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214646
Listing Expiration
2026-12-31
Marketing Start
2023-06-16
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71839112
Hyphenated Format
71839-112
Supplemental Identifiers
RxCUI
UPC
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
enoxaparin sodium (source: ndc)
Generic Name
enoxaparin sodium (source: ndc)
Application Number
ANDA214646 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 80 mg/.8mL
Packaging
- 10 SYRINGE in 1 CARTON (71839-112-10) / .8 mL in 1 SYRINGE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "5db5abf2-d207-4e03-a5cc-8e31f2fa20c0", "openfda": {"upc": ["0371839116102", "0371839115105"], "unii": ["8NZ41MIK1O"], "rxcui": ["854228", "854235", "854238", "854241", "854245", "854248", "854252"], "spl_set_id": ["b7197534-1daa-42de-8b83-a727da1195bf"], "manufacturer_name": ["BE Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 SYRINGE in 1 CARTON (71839-112-10) / .8 mL in 1 SYRINGE", "package_ndc": "71839-112-10", "marketing_start_date": "20230616"}], "brand_name": "enoxaparin sodium", "product_id": "71839-112_5db5abf2-d207-4e03-a5cc-8e31f2fa20c0", "dosage_form": "INJECTION", "pharm_class": ["Heparin", "Low-Molecular-Weight [CS]", "Low Molecular Weight Heparin [EPC]"], "product_ndc": "71839-112", "generic_name": "enoxaparin sodium", "labeler_name": "BE Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "enoxaparin sodium", "active_ingredients": [{"name": "ENOXAPARIN SODIUM", "strength": "80 mg/.8mL"}], "application_number": "ANDA214646", "marketing_category": "ANDA", "marketing_start_date": "20230616", "listing_expiration_date": "20261231"}