Hydrocodone Bitartrate and Acetaminophen
- Product NDC
- 71335-2116
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocodone Bitartrate and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210211
- Marketing category
- ANDA
- Substance
- ACETAMINOPHEN; HYDROCODONE BITARTRATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71335-2116-1 | 30 TABLET in 1 BOTTLE (71335-2116-1) | 20240906 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| 65c5abc7-520a-4267-acb6-ea6204a3ecfa | Hydrocodone Bitartrate and Acetaminophen Tablets, USP CII Revised: 01/2024 | Bryant Ranch Prepack | 2024-09-06 | HUMAN PRESCRIPTION DRUG LABEL | 102 |