Package 71335-2710-1

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2710-1
Digits Only 7133527101
Product NDC 71335-2710
Product ID 71335-2710_68da8a88-e635-48d5-bf65-768feb57d29e
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2710-1)

Marketing

Marketing Status
Marketed Since 2025-07-28
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": "68da8a88-e635-48d5-bf65-768feb57d29e", "openfda": {"unii": ["0020414E5U"], "rxcui": ["629699"], "spl_set_id": ["2688e63a-09c7-4d73-a923-cf14fec7b1a4"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2710-1)", "package_ndc": "71335-2710-1", "marketing_start_date": "20250728"}], "brand_name": "Minocycline Hydrochloride", "product_id": "71335-2710_68da8a88-e635-48d5-bf65-768feb57d29e", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "71335-2710", "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": "90 mg/1"}], "application_number": "ANDA204453", "marketing_category": "ANDA", "marketing_start_date": "20160930", "listing_expiration_date": "20261231"}