enoxaparin sodium
Generic: enoxaparin sodium
Labeler: amphastar pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
enoxaparin sodium
Generic Name
enoxaparin sodium
Labeler
amphastar pharmaceuticals, inc.
Dosage Form
INJECTION
Routes
Active Ingredients
enoxaparin sodium 100 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0548-5601
Product ID
0548-5601_2910408b-d506-4a3a-a2c8-64fc46ba0da0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076684
Listing Expiration
2026-12-31
Marketing Start
2011-09-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05485601
Hyphenated Format
0548-5601
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
enoxaparin sodium (source: ndc)
Generic Name
enoxaparin sodium (source: ndc)
Application Number
ANDA076684 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/mL
Packaging
- 10 SYRINGE in 1 CARTON (0548-5601-00) / .3 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": "2910408b-d506-4a3a-a2c8-64fc46ba0da0", "openfda": {"unii": ["8NZ41MIK1O"], "rxcui": ["854228", "854235", "854238", "854241", "854245", "854248", "854252", "854255"], "spl_set_id": ["3e6bf2b3-9339-4104-bda3-ad86a1949703"], "manufacturer_name": ["Amphastar Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 SYRINGE in 1 CARTON (0548-5601-00) / .3 mL in 1 SYRINGE", "package_ndc": "0548-5601-00", "marketing_start_date": "20110919"}], "brand_name": "Enoxaparin Sodium", "product_id": "0548-5601_2910408b-d506-4a3a-a2c8-64fc46ba0da0", "dosage_form": "INJECTION", "pharm_class": ["Heparin", "Low-Molecular-Weight [CS]", "Low Molecular Weight Heparin [EPC]"], "product_ndc": "0548-5601", "generic_name": "Enoxaparin sodium", "labeler_name": "Amphastar Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enoxaparin Sodium", "active_ingredients": [{"name": "ENOXAPARIN SODIUM", "strength": "100 mg/mL"}], "application_number": "ANDA076684", "marketing_category": "ANDA", "marketing_start_date": "20110919", "listing_expiration_date": "20261231"}