Package 60687-921-21

Brand: norethindrone acetate

Generic: norethindrone acetate
NDC Package

Package Facts

Identity

Package NDC 60687-921-21
Digits Only 6068792121
Product NDC 60687-921
Product ID 60687-921_485ceb49-adae-1b29-e063-6294a90aded8
Description

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

Marketing

Marketing Status
Marketed Since 2026-01-14
Brand norethindrone acetate
Generic norethindrone acetate
Sample Package No

Linked Drug Pages (1)

Norethindrone Acetate ndc-match (0.95)

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"}