Package 63629-1177-1
Brand: hydrocodone bitartrate and acetaminophen
Generic: hydrocodone bitartrate and acetaminophenPackage Facts
Identity
Package NDC
63629-1177-1
Digits Only
6362911771
Product NDC
63629-1177
Description
100 TABLET in 1 BOTTLE (63629-1177-1)
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": "fc12f03d-145a-f3cf-e053-6294a90aa85b", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["856987"], "spl_set_id": ["2f6d0712-e756-49f2-a6b8-bbd160a454c4"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-1177-1)", "package_ndc": "63629-1177-1", "marketing_start_date": "20190617"}], "brand_name": "hydrocodone bitartrate and acetaminophen", "product_id": "63629-1177_fc12f03d-145a-f3cf-e053-6294a90aa85b", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "63629-1177", "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": "300 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "5 mg/1"}], "application_number": "ANDA207509", "marketing_category": "ANDA", "marketing_start_date": "20190617", "listing_expiration_date": "20261231"}