Hydrocodone Bitartrate and Acetaminophen

Product NDC
71335-9602
11-digit product format
713359602
Labeler code
71335
Product ID
71335-9602_3674bbec-4d22-49a2-b7cf-5c50d9177f3e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydrocodone Bitartrate and Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA211487
Marketing category
ANDA
Marketing start
2018-11-08
Substance
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Active strength
325; 10 mg/1; mg/1
Pharmacologic classes
Opioid Agonist [EPC], Opioid Agonists [MoA]
DEA schedule
CII
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
362O9ITL9DACETAMINOPHEN103-90-2ACETAMINOPHEN
NO70W886KKHYDROCODONE BITARTRATE34195-34-1HYDROCODONE BITARTRATE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-9602-17133596020121 TABLET in 1 BOTTLE (71335-9602-1) 21 tablet2022-12-12NoNoHistorical
71335-9602-27133596020215 TABLET in 1 BOTTLE (71335-9602-2) 15 tablet2022-12-12NoNoHistorical
71335-9602-37133596020310 TABLET in 1 BOTTLE (71335-9602-3) 10 tablet2022-12-12NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
® TabletsBryant Ranch Prepack2025-10-24HUMAN PRESCRIPTION DRUG LABEL102
® TabletsBryant Ranch Prepack2023-11-10HUMAN PRESCRIPTION DRUG LABEL101