Package 63629-9208-1

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-9208-1
Digits Only 6362992081
Product NDC 63629-9208
Product ID 63629-9208_9c51636a-8232-4acf-8541-8752d8b6b72e
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9208-1)

Marketing

Marketing Status
Marketed Since 2022-03-02
Brand minocycline hydrochloride
Generic minocycline hydrochloride
Sample Package No

Linked Drug Pages (1)

Minocycline Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9c51636a-8232-4acf-8541-8752d8b6b72e", "openfda": {"unii": ["0020414E5U"], "rxcui": ["1013659"], "spl_set_id": ["6e0efd1a-5a09-4030-8fe2-f98334cdeb0e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9208-1)", "package_ndc": "63629-9208-1", "marketing_start_date": "20220302"}], "brand_name": "Minocycline Hydrochloride", "product_id": "63629-9208_9c51636a-8232-4acf-8541-8752d8b6b72e", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "63629-9208", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "105 mg/1"}], "application_number": "ANDA204453", "marketing_category": "ANDA", "marketing_start_date": "20160930", "listing_expiration_date": "20261231"}