Package 63629-9213-1

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-9213-1
Digits Only 6362992131
Product NDC 63629-9213
Product ID 63629-9213_931b98ea-4357-4202-90a6-20521845b250
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9213-1)

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": "931b98ea-4357-4202-90a6-20521845b250", "openfda": {"unii": ["0020414E5U"], "rxcui": ["858372"], "spl_set_id": ["dddad9bc-a0a3-41bf-81e5-65d9903b14c6"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9213-1)", "package_ndc": "63629-9213-1", "marketing_start_date": "20220302"}], "brand_name": "Minocycline Hydrochloride", "product_id": "63629-9213_931b98ea-4357-4202-90a6-20521845b250", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "63629-9213", "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": "65 mg/1"}], "application_number": "ANDA204453", "marketing_category": "ANDA", "marketing_start_date": "20160930", "listing_expiration_date": "20261231"}