Hydrocodone Bitartrate and Acetaminophen

Product NDC
71335-2104
11-digit product format
713352104
Labeler code
71335
Product ID
71335-2104_60dff6ef-c813-4e21-8cdd-38e5217ce34c
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; 7.5 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
71335-2104-17133521040130 TABLET in 1 BOTTLE (71335-2104-1) 30 tablet2022-06-06NoNoHistorical
71335-2104-27133521040215 TABLET in 1 BOTTLE (71335-2104-2) 15 tablet2022-06-06NoNoHistorical
71335-2104-37133521040328 TABLET in 1 BOTTLE (71335-2104-3) 28 tablet2022-06-06NoNoHistorical
71335-2104-47133521040456 TABLET in 1 BOTTLE (71335-2104-4) 56 tablet2022-06-06NoNoHistorical
71335-2104-57133521040560 TABLET in 1 BOTTLE (71335-2104-5) 60 tablet2022-06-06NoNoHistorical
71335-2104-67133521040690 TABLET in 1 BOTTLE (71335-2104-6) 90 tablet2022-06-06NoNoHistorical
71335-2104-771335210407120 TABLET in 1 BOTTLE (71335-2104-7) 120 tablet2022-06-06NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
® TabletsBryant Ranch Prepack2025-10-08HUMAN PRESCRIPTION DRUG LABEL102
® TabletsBryant Ranch Prepack2023-10-26HUMAN PRESCRIPTION DRUG LABEL101