Package 70518-1336-1

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1336-1
Digits Only 7051813361
Product NDC 70518-1336
Product ID 70518-1336_48d74037-829a-f6bc-e063-6294a90a7d50
Description

30 CAPSULE in 1 BLISTER PACK (70518-1336-1)

Marketing

Marketing Status
Marketed Since 2018-08-21
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": "48d74037-829a-f6bc-e063-6294a90a7d50", "openfda": {"unii": ["0020414E5U"], "rxcui": ["197984"], "spl_set_id": ["0becbde8-6ec5-4830-a0d9-cfdb7b15eb84"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-1336-1)", "package_ndc": "70518-1336-1", "marketing_start_date": "20180821"}], "brand_name": "Minocycline Hydrochloride", "product_id": "70518-1336_48d74037-829a-f6bc-e063-6294a90a7d50", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70518-1336", "generic_name": "Minocycline Hydrochloride", "labeler_name": "REMEDYREPACK 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": "20180801", "listing_expiration_date": "20271231"}