Package 71930-027-43

Brand: hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 71930-027-43
Digits Only 7193002743
Product NDC 71930-027
Product ID 71930-027_5ab6fc05-d708-4f00-9336-33a541bf0c87
Description

473 mL in 1 BOTTLE (71930-027-43)

Marketing

Marketing Status
Marketed Since 2019-04-08
Brand hydrocodone bitartrate and acetaminophen
Generic hydrocodone bitartrate and acetaminophen
Sample Package No

Linked Drug Pages (1)

Hydrocodone Bitartrate and Acetaminophen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5ab6fc05-d708-4f00-9336-33a541bf0c87", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["856940"], "spl_set_id": ["adb37532-aa19-48a2-95a1-8c92a6ce8651"], "manufacturer_name": ["Eywa Pharma Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (71930-027-43)", "package_ndc": "71930-027-43", "marketing_start_date": "20190408"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "71930-027_5ab6fc05-d708-4f00-9336-33a541bf0c87", "dosage_form": "SOLUTION", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "71930-027", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Eywa Pharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/15mL"}, {"name": "HYDROCODONE BITARTRATE", "strength": "7.5 mg/15mL"}], "application_number": "ANDA211023", "marketing_category": "ANDA", "marketing_start_date": "20190408", "listing_expiration_date": "20261231"}