Hydrocodone Bitartrate and Acetaminophen
- Product NDC
- 67296-1335
- 11-digit product format
- 672961335
- Labeler code
- 67296
- Product ID
- 67296-1335_d611392d-9fd8-c014-e053-2a95a90a33e2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocodone Bitartrate and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA202991
- Marketing category
- ANDA
- Marketing start
- 2016-04-12
- 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 |
|---|
| 67296-1335-1 | Hydrocodone Bitartrate and Acetaminophen | 10 in 1 BOTTLE | TABLET | 10 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1335 | HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [REDPHARM DRUG, INC.] | 4 | Legacy NDC, 1 package rows | 20220121_503457f0-7e83-56c8-e054-00144ff88e88.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 |
|---|
| 67296-1335-1 | 67296133501 | 10 TABLET in 1 BOTTLE (67296-1335-1) | 10 tablet | 2016-04-12 | 0000-00-00 | No | No | Current |