Package 0904-6888-06

Brand: minocycline hydrochloride

Generic: minocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-6888-06
Digits Only 0904688806
Product NDC 0904-6888
Product ID 0904-6888_aed0618f-2e64-4e18-991b-1e38efcf56b2
Description

50 BLISTER PACK in 1 CARTON (0904-6888-06) / 1 CAPSULE in 1 BLISTER PACK

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": "aed0618f-2e64-4e18-991b-1e38efcf56b2", "openfda": {"unii": ["0020414E5U"], "rxcui": ["197984"], "spl_set_id": ["fd86ff45-37d0-4501-b9fb-e1836e4a8be4"], "manufacturer_name": ["Major Pharamceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-6888-06)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-6888-06", "marketing_start_date": "20150402"}], "brand_name": "Minocycline Hydrochloride", "product_id": "0904-6888_aed0618f-2e64-4e18-991b-1e38efcf56b2", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "0904-6888", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Major Pharamceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA065062", "marketing_category": "ANDA", "marketing_start_date": "20150402", "listing_expiration_date": "20261231"}