enoxaparin sodium
Generic: enoxaparin sodium
Labeler: sanofi-aventis u.s. llcDrug Facts
Product Profile
Brand Name
enoxaparin sodium
Generic Name
enoxaparin sodium
Labeler
sanofi-aventis u.s. llc
Dosage Form
INJECTION
Routes
Active Ingredients
enoxaparin sodium 80 mg/.8mL
Manufacturer
Identifiers & Regulatory
Product NDC
0955-1008
Product ID
0955-1008_48bacfb7-7152-45b1-a188-59c4a205f5b0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA020164
Listing Expiration
2027-12-31
Marketing Start
2011-10-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09551008
Hyphenated Format
0955-1008
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
NDA020164 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 80 mg/.8mL
Packaging
- 10 CELLO PACK in 1 CARTON (0955-1008-10) / 1 SYRINGE in 1 CELLO PACK (0955-1008-01) / .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": "48bacfb7-7152-45b1-a188-59c4a205f5b0", "openfda": {"unii": ["8NZ41MIK1O"], "rxcui": ["854228", "854235", "854238", "854241", "854245", "854248", "854252", "854255"], "spl_set_id": ["20635579-c92d-4f6c-a332-1096d51002f2"], "manufacturer_name": ["Sanofi-Aventis U.S. LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 CELLO PACK in 1 CARTON (0955-1008-10) / 1 SYRINGE in 1 CELLO PACK (0955-1008-01) / .8 mL in 1 SYRINGE", "package_ndc": "0955-1008-10", "marketing_start_date": "20111003"}], "brand_name": "Enoxaparin sodium", "product_id": "0955-1008_48bacfb7-7152-45b1-a188-59c4a205f5b0", "dosage_form": "INJECTION", "pharm_class": ["Heparin", "Low-Molecular-Weight [CS]", "Low Molecular Weight Heparin [EPC]"], "product_ndc": "0955-1008", "generic_name": "enoxaparin sodium", "labeler_name": "Sanofi-Aventis U.S. LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enoxaparin sodium", "active_ingredients": [{"name": "ENOXAPARIN SODIUM", "strength": "80 mg/.8mL"}], "application_number": "NDA020164", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20111003", "listing_expiration_date": "20271231"}