norethindrone acetate
Generic: norethindrone acetate
Labeler: golden state medical supply, inc.Drug Facts
Product Profile
Brand Name
norethindrone acetate
Generic Name
norethindrone acetate
Labeler
golden state medical supply, inc.
Dosage Form
TABLET
Routes
Active Ingredients
norethindrone acetate 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51407-599
Product ID
51407-599_2bb2a27e-11f5-a9fb-e063-6394a90a1ea8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075951
Listing Expiration
2026-12-31
Marketing Start
2001-05-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51407599
Hyphenated Format
51407-599
Supplemental Identifiers
RxCUI
UNII
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
norethindrone acetate (source: ndc)
Generic Name
norethindrone acetate (source: ndc)
Application Number
ANDA075951 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 50 TABLET in 1 BOTTLE (51407-599-50)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2bb2a27e-11f5-a9fb-e063-6394a90a1ea8", "openfda": {"unii": ["9S44LIC7OJ"], "rxcui": ["1000405"], "spl_set_id": ["2bb29135-6e9b-a9e2-e063-6394a90ae9e4"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (51407-599-50)", "package_ndc": "51407-599-50", "marketing_start_date": "20241220"}], "brand_name": "Norethindrone Acetate", "product_id": "51407-599_2bb2a27e-11f5-a9fb-e063-6394a90a1ea8", "dosage_form": "TABLET", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "51407-599", "generic_name": "Norethindrone Acetate", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norethindrone Acetate", "active_ingredients": [{"name": "NORETHINDRONE ACETATE", "strength": "5 mg/1"}], "application_number": "ANDA075951", "marketing_category": "ANDA", "marketing_start_date": "20010525", "listing_expiration_date": "20261231"}