HYDROCODONE BITARTRATE AND ACETAMINOPHEN
- Product NDC
- 67296-1238
- 11-digit product format
- 672961238
- Labeler code
- 67296
- Product ID
- 67296-1238_9c9f1f5c-86b2-15d3-e053-2995a90afc6e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYDROCODONE BITARTRATE AND ACETAMINOPHEN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA090118
- Marketing category
- ANDA
- Marketing start
- 2009-03-30
- 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
- 2021-12-31
- 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 |
|---|
| 67296-1238-2 | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | 20 in 1 BOTTLE | TABLET | 20 | | 4 |
| 67296-1238-3 | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | 30 in 1 BOTTLE | TABLET | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1238 | HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET [REDPHARM DRUG, INC.] | 4 | Legacy NDC, 2 package rows | 20200123_4f42bbd5-9b62-3ec9-e054-00144ff8d46c.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 |
|---|
| 67296-1238-2 | 67296123802 | 20 TABLET in 1 BOTTLE (67296-1238-2) | 20 tablet | 2009-03-30 | 0000-00-00 | No | No | Current |
| 67296-1238-3 | 67296123803 | 30 TABLET in 1 BOTTLE (67296-1238-3) | 30 tablet | 2009-03-30 | 0000-00-00 | No | No | Current |