"79739-7182-1" National Drug Code (NDC)

NDC Code	79739-7182-1
Package Description	100 TABLET in 1 BOTTLE (79739-7182-1)
Product NDC	79739-7182
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Hydrocodone Bitartrate And Aspirin
Non-Proprietary Name	Hydrocodone Bitartrate And Aspirin
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20210528
Marketing Category Name	ANDA
Application Number	ANDA205479
Manufacturer	LGM PHARMA SOLUTIONS, LLC
Substance Name	ASPIRIN; HYDROCODONE BITARTRATE
Strength	500; 5
Strength Unit	mg/1; mg/1
Pharmacy Classes	Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Opioid Agonist [EPC], Opioid Agonists [MoA], Platelet Aggregation Inhibitor [EPC]
DEA Schedule	CII