Package 71335-2904-1

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2904-1
Digits Only 7133529041
Product NDC 71335-2904
Product ID 71335-2904_604b1b63-915a-47fc-a311-e668fcebd05a
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2904-1)

Marketing

Marketing Status
Marketed Since 2025-11-07
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": "604b1b63-915a-47fc-a311-e668fcebd05a", "openfda": {"unii": ["0020414E5U"], "rxcui": ["1013659"], "spl_set_id": ["c11bfea8-6079-44ce-b8e1-20bfba631bec"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2904-1)", "package_ndc": "71335-2904-1", "marketing_start_date": "20251107"}], "brand_name": "Minocycline Hydrochloride", "product_id": "71335-2904_604b1b63-915a-47fc-a311-e668fcebd05a", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "71335-2904", "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"}