Package 68071-3685-6
Brand: hydrocodone bitartrate and acetaminophen
Generic: hydrocodone bitartrate and acetaminophenPackage Facts
Identity
Package NDC
68071-3685-6
Digits Only
6807136856
Product NDC
68071-3685
Description
6 TABLET in 1 BOTTLE, PLASTIC (68071-3685-6)
Marketing
Marketing Status
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": "226765d3-3226-2302-e063-6394a90a27a9", "openfda": {"upc": ["0368071368567"], "unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857002"], "spl_set_id": ["226765e9-a6b1-22b6-e063-6394a90a364e"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (68071-3685-6)", "package_ndc": "68071-3685-6", "marketing_start_date": "20240918"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "68071-3685_226765d3-3226-2302-e063-6394a90a27a9", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "68071-3685", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "5 mg/1"}], "application_number": "ANDA202214", "marketing_category": "ANDA", "marketing_start_date": "20141006", "listing_expiration_date": "20261231"}