norethindrone acetate

Generic: norethindrone acetate

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name norethindrone acetate
Generic Name norethindrone acetate
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

norethindrone acetate 5 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-921
Product ID 60687-921_485ceb49-adae-1b29-e063-6294a90aded8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091090
Listing Expiration 2027-12-31
Marketing Start 2026-01-14

Pharmacologic Class

Classes
progesterone congeners [cs] progestin [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687921
Hyphenated Format 60687-921

Supplemental Identifiers

RxCUI
1000405
UNII
9S44LIC7OJ

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 ANDA091090 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (60687-921-21) / 1 TABLET in 1 BLISTER PACK (60687-921-11)
source: ndc

Packages (1)

60687-921-21 30 BLISTER PACK in 1 CARTON (60687-921-21) / 1 TABLET in 1 BLISTER PACK (60687-921-11)

Ingredients (1)

norethindrone acetate (5 mg/1)

Linked Drug Pages (1)

Norethindrone Acetate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "485ceb49-adae-1b29-e063-6294a90aded8", "openfda": {"unii": ["9S44LIC7OJ"], "rxcui": ["1000405"], "spl_set_id": ["eb0b80e0-5b69-4efa-ae8a-62e718a62dc3"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-921-21)  / 1 TABLET in 1 BLISTER PACK (60687-921-11)", "package_ndc": "60687-921-21", "marketing_start_date": "20260114"}], "brand_name": "Norethindrone Acetate", "product_id": "60687-921_485ceb49-adae-1b29-e063-6294a90aded8", "dosage_form": "TABLET", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "60687-921", "generic_name": "Norethindrone Acetate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norethindrone Acetate", "active_ingredients": [{"name": "NORETHINDRONE ACETATE", "strength": "5 mg/1"}], "application_number": "ANDA091090", "marketing_category": "ANDA", "marketing_start_date": "20260114", "listing_expiration_date": "20271231"}