Package 68382-318-18
Brand: minocycline hydrochloride
Generic: minocycline hydrochloridePackage Facts
Identity
Package NDC
68382-318-18
Digits Only
6838231818
Product NDC
68382-318
Description
50 CAPSULE in 1 BOTTLE (68382-318-18)
Marketing
Marketing Status
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": "50 CAPSULE in 1 BOTTLE (68382-318-18)", "package_ndc": "68382-318-18", "marketing_start_date": "20170403"}], "brand_name": "Minocycline hydrochloride", "product_id": "68382-318_0c236c6b-5f2a-4b46-a12f-45c47b90b65a", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "68382-318", "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": "100 mg/1"}], "application_number": "ANDA063009", "marketing_category": "ANDA", "marketing_start_date": "20170403", "listing_expiration_date": "20261231"}