Package 0009-0065-01

Brand: provera

Generic: medroxyprogesterone acetate
NDC Package

Package Facts

Identity

Package NDC 0009-0065-01
Digits Only 0009006501
Product NDC 0009-0065
Product ID 0009-0065_80c81ad8-3d42-4a21-ac4c-d331bc5e4956
Description

100 TABLET in 1 BOTTLE (0009-0065-01)

Marketing

Marketing Status
Marketed Since 2019-09-03
Brand provera
Generic medroxyprogesterone acetate
Sample Package No

Linked Drug Pages (1)

Provera ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "80c81ad8-3d42-4a21-ac4c-d331bc5e4956", "openfda": {"unii": ["C2QI4IOI2G"], "rxcui": ["1000114", "1000124", "1000135", "1000139", "1000141", "1000145"], "spl_set_id": ["a586be28-96af-4fed-a13f-9b94fd4c7405"], "manufacturer_name": ["Pharmacia & Upjohn Company LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0009-0065-01)", "package_ndc": "0009-0065-01", "marketing_start_date": "20190903"}], "brand_name": "Provera", "product_id": "0009-0065_80c81ad8-3d42-4a21-ac4c-d331bc5e4956", "dosage_form": "TABLET", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "0009-0065", "generic_name": "medroxyprogesterone acetate", "labeler_name": "Pharmacia & Upjohn Company LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Provera", "active_ingredients": [{"name": "MEDROXYPROGESTERONE ACETATE", "strength": "2.5 mg/1"}], "application_number": "NDA011839", "marketing_category": "NDA", "marketing_start_date": "20190903", "listing_expiration_date": "20261231"}