Hydrocodone Bitartrate and Acetaminophen
- Product NDC
- 67296-1618
- 11-digit product format
- 672961618
- Labeler code
- 67296
- Product ID
- 67296-1618_d61efbf7-ae60-8311-e053-2a95a90a40ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocodone Bitartrate and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA209037
- Marketing category
- ANDA
- Marketing start
- 2018-01-01
- 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1618-1 | 67296161801 | 10 TABLET in 1 BOTTLE (67296-1618-1) | 10 tablet | 2020-01-01 | 0000-00-00 | No | No | Current |
| 67296-1618-3 | 67296161803 | 30 TABLET in 1 BOTTLE (67296-1618-3) | 30 tablet | 2020-01-01 | 0000-00-00 | No | No | Current |
| 67296-1618-6 | 67296161806 | 6 TABLET in 1 BOTTLE (67296-1618-6) | 6 tablet | 2018-01-01 | 0000-00-00 | No | No | Current |
| 67296-1618-9 | 67296161809 | 12 TABLET in 1 BOTTLE (67296-1618-9) | 12 tablet | 2018-01-01 | 0000-00-00 | No | No | Current |