Hydrocodone Bitartrate and Acetaminophen
- Product NDC
- 68071-3685
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocodone Bitartrate and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA202214
- Marketing category
- ANDA
- Substance
- ACETAMINOPHEN; HYDROCODONE BITARTRATE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 68071-3685-6 | 6 TABLET in 1 BOTTLE, PLASTIC (68071-3685-6) | 2024-09-18 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Hydrocodone Bitartrate and Acetaminophen | NuCare Pharmaceuticals, Inc. | 2024-09-18 | HUMAN PRESCRIPTION DRUG LABEL | 1 |