Package 63187-778-20

Brand: hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 63187-778-20
Digits Only 6318777820
Product NDC 63187-778
Description

20 TABLET in 1 BOTTLE (63187-778-20)

Marketing

Marketing Status
Marketed Since 2016-11-01
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": "156868e3-86ea-4689-90b4-734d29634b29", "openfda": {"upc": ["0363187778309"], "unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["856999"], "spl_set_id": ["199d4915-cb3b-48f3-835d-a45d04a5c940"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE (63187-778-12)", "package_ndc": "63187-778-12", "marketing_start_date": "20161101"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (63187-778-15)", "package_ndc": "63187-778-15", "marketing_start_date": "20170201"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (63187-778-20)", "package_ndc": "63187-778-20", "marketing_start_date": "20161101"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-778-30)", "package_ndc": "63187-778-30", "marketing_start_date": "20161101"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-778-60)", "package_ndc": "63187-778-60", "marketing_start_date": "20161101"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-778-90)", "package_ndc": "63187-778-90", "marketing_start_date": "20170201"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "63187-778_156868e3-86ea-4689-90b4-734d29634b29", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "63187-778", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA201013", "marketing_category": "ANDA", "marketing_start_date": "20120412", "listing_expiration_date": "20261231"}