Package 50268-400-15

Brand: hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 50268-400-15
Digits Only 5026840015
Product NDC 50268-400
Description

50 BLISTER PACK in 1 BOX (50268-400-15) / 1 TABLET in 1 BLISTER PACK (50268-400-11)

Marketing

Marketing Status
Marketed Since 2016-10-28
Brand hydrocodone bitartrate and acetaminophen
Generic hydrocodone bitartrate and acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47e5550b-f34a-dda4-e063-6294a90affee", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857005"], "spl_set_id": ["678f3d54-3b62-c9e8-2ff3-a2a6bd9ecfc3"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-400-15)  / 1 TABLET in 1 BLISTER PACK (50268-400-11)", "package_ndc": "50268-400-15", "marketing_start_date": "20161028"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "50268-400_47e5550b-f34a-dda4-e063-6294a90affee", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "50268-400", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "7.5 mg/1"}], "application_number": "ANDA040746", "marketing_category": "ANDA", "marketing_start_date": "20161028", "listing_expiration_date": "20271231"}