Package 63629-9210-1

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-9210-1
Digits Only 6362992101
Product NDC 63629-9210
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9210-1)

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b88e6ee2-70d3-4d6a-bdff-1cafbb2b9daf", "openfda": {"unii": ["0020414E5U"], "rxcui": ["629695"], "spl_set_id": ["fb4deae8-23f0-42dd-ac2e-b69ab39a6c4d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9210-1)", "package_ndc": "63629-9210-1", "marketing_start_date": "20220302"}], "brand_name": "Minocycline Hydrochloride", "product_id": "63629-9210_b88e6ee2-70d3-4d6a-bdff-1cafbb2b9daf", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "63629-9210", "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": "135 mg/1"}], "application_number": "ANDA204453", "marketing_category": "ANDA", "marketing_start_date": "20160930", "listing_expiration_date": "20261231"}