Package 68382-317-01

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68382-317-01
Digits Only 6838231701
Product NDC 68382-317
Description

100 CAPSULE in 1 BOTTLE (68382-317-01)

Marketing

Marketing Status
Marketed Since 2017-04-03
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": "0c236c6b-5f2a-4b46-a12f-45c47b90b65a", "openfda": {"unii": ["0020414E5U"], "rxcui": ["197984", "197985", "314108"], "spl_set_id": ["25acb785-6838-4e62-9e86-ddc30b2b759a"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68382-317-01)", "package_ndc": "68382-317-01", "marketing_start_date": "20170403"}], "brand_name": "Minocycline hydrochloride", "product_id": "68382-317_0c236c6b-5f2a-4b46-a12f-45c47b90b65a", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "68382-317", "generic_name": "Minocycline hydrochloride", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA063009", "marketing_category": "ANDA", "marketing_start_date": "20170403", "listing_expiration_date": "20261231"}