Hydrocodone Bitartrate and Acetaminophen

Product NDC
63187-375
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydrocodone Bitartrate and Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA201013
Marketing category
ANDA
Substance
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
63187-375-1212 TABLET in 1 BOTTLE (63187-375-12) 2022-02-08NoHistorical
63187-375-1515 TABLET in 1 BOTTLE (63187-375-15) 2016-09-01NoHistorical
63187-375-2020 TABLET in 1 BOTTLE (63187-375-20) 2016-09-01NoHistorical
63187-375-3030 TABLET in 1 BOTTLE (63187-375-30) 2016-09-01NoHistorical
63187-375-6060 TABLET in 1 BOTTLE (63187-375-60) 2016-09-01NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Hydrocodone Bitartrate and Acetaminophen Tablets, USPProficient Rx LP2023-04-01HUMAN PRESCRIPTION DRUG LABEL6