Package 63629-2292-1
Brand: hydrocodone bitartrate and acetaminophen
Generic: hydrocodone bitartrate and acetaminophenPackage Facts
Identity
Package NDC
63629-2292-1
Digits Only
6362922921
Product NDC
63629-2292
Description
100 TABLET in 1 BOTTLE, PLASTIC (63629-2292-1)
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": "da66eb8f-0e25-4283-b13e-b8a63e9ce3f9", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857002"], "spl_set_id": ["2ad2d00e-3796-4605-852f-a3d64d5ef09f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (63629-2292-1)", "package_ndc": "63629-2292-1", "marketing_start_date": "20141006"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "63629-2292_da66eb8f-0e25-4283-b13e-b8a63e9ce3f9", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "63629-2292", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "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"}