Package 68071-2225-8

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-2225-8
Digits Only 6807122258
Product NDC 68071-2225
Description

28 CAPSULE in 1 BOTTLE (68071-2225-8)

Marketing

Marketing Status
Marketed Since 2020-07-30
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": "1d7632a7-0f25-9e5d-e063-6294a90ad21f", "openfda": {"upc": ["0368071222586"], "unii": ["0020414E5U"], "rxcui": ["197984"], "spl_set_id": ["abaacdeb-2433-261a-e053-2995a90ae34e"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "28 CAPSULE in 1 BOTTLE (68071-2225-8)", "package_ndc": "68071-2225-8", "marketing_start_date": "20200730"}], "brand_name": "Minocycline Hydrochloride", "product_id": "68071-2225_1d7632a7-0f25-9e5d-e063-6294a90ad21f", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "68071-2225", "generic_name": "Minocycline Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA065470", "marketing_category": "ANDA", "marketing_start_date": "20080311", "listing_expiration_date": "20261231"}