Package 13668-487-50

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 13668-487-50
Digits Only 1366848750
Product NDC 13668-487
Product ID 13668-487_c0e490fa-abbc-4c43-be4d-f1dd077eb0a1
Description

50 TABLET in 1 BOTTLE (13668-487-50)

Marketing

Marketing Status
Marketed Since 2015-04-02
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": "c0e490fa-abbc-4c43-be4d-f1dd077eb0a1", "openfda": {"upc": ["0313668487503", "0313668486018"], "unii": ["0020414E5U"], "rxcui": ["207362", "207364", "403840"], "spl_set_id": ["3539f84e-b489-4914-96c1-ac3731032971"], "manufacturer_name": ["Torrent Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (13668-487-50)", "package_ndc": "13668-487-50", "marketing_start_date": "20150402"}], "brand_name": "MINOCYCLINE HYDROCHLORIDE", "product_id": "13668-487_c0e490fa-abbc-4c43-be4d-f1dd077eb0a1", "dosage_form": "TABLET", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "13668-487", "generic_name": "MINOCYCLINE HYDROCHLORIDE", "labeler_name": "Torrent Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MINOCYCLINE HYDROCHLORIDE", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA065156", "marketing_category": "ANDA", "marketing_start_date": "20150402", "listing_expiration_date": "20261231"}