Hydrocodone Bitartrate and Acetaminophen
- Product NDC
- 67296-1705
- 11-digit product format
- 672961705
- Labeler code
- 67296
- Product ID
- 67296-1705_b8dfb538-7987-5311-e053-2995a90a07bd
- 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
- 2019-11-01
- Marketing end
- 0000-00-00
- Substance
- HYDROCODONE BITARTRATE; ACETAMINOPHEN
- Active strength
- 8 mg/1; mg/1
- Pharmacologic classes
- Opioid Agonist [EPC],Opioid Agonists [MoA]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 67296-1705-3 | Hydrocodone Bitartrate and Acetaminophen | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 67296-1705-6 | Hydrocodone Bitartrate and Acetaminophen | 6 in 1 BOTTLE | TABLET | 6 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1705 | HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 2 package rows | 20240805_96ca2ab0-d4e7-63f2-e053-2995a90ae28c.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 |
|---|
| 67296-1705-3 | 67296170503 | 30 TABLET in 1 BOTTLE (67296-1705-3) | 30 tablet | 2019-11-01 | 0000-00-00 | No | No | Current |
| 67296-1705-6 | 67296170506 | 6 TABLET in 1 BOTTLE (67296-1705-6) | 6 tablet | 2019-11-01 | 0000-00-00 | No | No | Current |