Package 0591-3153-01

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0591-3153-01
Digits Only 0591315301
Product NDC 0591-3153
Description

100 CAPSULE in 1 BOTTLE, PLASTIC (0591-3153-01)

Marketing

Marketing Status
Discontinued 2026-07-31
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": "2d74faa2-99c4-4f01-adc6-60110d2b24da", "openfda": {"upc": ["0305915694017"], "unii": ["0020414E5U"], "rxcui": ["197984", "197985", "314108"], "spl_set_id": ["a5fc4d50-50b2-46e0-b722-4c6b2ec47d06"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (0591-3153-01)", "package_ndc": "0591-3153-01", "marketing_end_date": "20260731", "marketing_start_date": "20020917"}], "brand_name": "Minocycline Hydrochloride", "product_id": "0591-3153_2d74faa2-99c4-4f01-adc6-60110d2b24da", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "0591-3153", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA063065", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20020917"}