Package 0009-0271-01

Brand: depo-estradiol

Generic: estradiol cypionate
NDC Package

Package Facts

Identity

Package NDC 0009-0271-01
Digits Only 0009027101
Product NDC 0009-0271
Product ID 0009-0271_70957ffe-7710-4a3a-98fa-bf5d84f38ddb
Description

1 VIAL in 1 CARTON (0009-0271-01) / 5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 1979-08-15
Brand depo-estradiol
Generic estradiol cypionate
Sample Package No

Linked Drug Pages (1)

Depo-Estradiol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR"], "spl_id": "70957ffe-7710-4a3a-98fa-bf5d84f38ddb", "openfda": {"unii": ["7E1DV054LO"], "rxcui": ["206417", "310187"], "spl_set_id": ["9a4229fd-fecd-4ac1-9c4f-6d442533457f"], "manufacturer_name": ["Pharmacia & Upjohn Company LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0009-0271-01)  / 5 mL in 1 VIAL", "package_ndc": "0009-0271-01", "marketing_start_date": "19790815"}], "brand_name": "Depo-Estradiol", "product_id": "0009-0271_70957ffe-7710-4a3a-98fa-bf5d84f38ddb", "dosage_form": "INJECTION", "pharm_class": ["Estradiol Congeners [CS]", "Estrogen Receptor Agonists [MoA]", "Estrogen [EPC]"], "product_ndc": "0009-0271", "generic_name": "estradiol cypionate", "labeler_name": "Pharmacia & Upjohn Company LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Depo-Estradiol", "active_ingredients": [{"name": "ESTRADIOL CYPIONATE", "strength": "5 mg/mL"}], "application_number": "ANDA085470", "marketing_category": "ANDA", "marketing_start_date": "19790815", "listing_expiration_date": "20261231"}