Hydrocodone Bitartrate and Acetaminophen
- Product NDC
- 67296-1794
- 11-digit product format
- 672961794
- Labeler code
- 67296
- Product ID
- 67296-1794_d61f51d8-4e86-a161-e053-2a95a90ad14a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocodone Bitartrate and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA211487
- Marketing category
- ANDA
- Marketing start
- 2018-11-08
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; HYDROCODONE BITARTRATE
- Active strength
- 325 mg/1; mg/1
- Pharmacologic classes
- Opioid Agonist [EPC], Opioid Agonists [MoA]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-1794-1 | Hydrocodone Bitartrate and Acetaminophen | 10 in 1 BOTTLE | TABLET | 10 | | 5 |
| 67296-1794-2 | Hydrocodone Bitartrate and Acetaminophen | 20 in 1 BOTTLE | TABLET | 20 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1794 | HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [REDPHARM DRUG, INC.] | 5 | Legacy NDC, 2 package rows | 20240727_afeba22b-fba8-d32a-e053-2995a90a4432.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1794-1 | 67296179401 | 10 TABLET in 1 BOTTLE (67296-1794-1) | 10 tablet | 2018-11-08 | 0000-00-00 | No | No | Current |
| 67296-1794-2 | 67296179402 | 20 TABLET in 1 BOTTLE (67296-1794-2) | 20 tablet | 2018-11-08 | 0000-00-00 | No | No | Current |