OXYCODONE AND ACETAMINOPHEN

Product NDC
76420-320
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Oxycodone and Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
Asclemed USA, Inc.
Application
ANDA207419
Marketing category
ANDA
Substance
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
76420-320-01100 TABLET in 1 BOTTLE (76420-320-01) 2025-04-15NoHistorical
76420-320-05500 TABLET in 1 BOTTLE (76420-320-05) 2025-04-15NoHistorical
76420-320-3030 TABLET in 1 BOTTLE (76420-320-30) 2025-04-15NoHistorical
76420-320-6060 TABLET in 1 BOTTLE (76420-320-60) 2025-04-15NoHistorical
76420-320-9090 TABLET in 1 BOTTLE (76420-320-90) 2025-04-15NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Oxycodone and Acetaminophen Tablets, USP CII Rx onlyAsclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM2025-04-15HUMAN PRESCRIPTION DRUG LABEL1