Oxycodone and Acetaminophen
- Product NDC
- 67296-1773
- 11-digit product format
- 672961773
- Labeler code
- 67296
- Product ID
- 67296-1773_d61cc7c2-88c5-400d-e053-2a95a90ad7e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA202677
- Marketing category
- ANDA
- Marketing start
- 2020-01-01
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
- Active strength
- 325 mg/1; mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA], Opioid Agonist [EPC]
- 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 |
|---|
| 67296-1773-6 | Oxycodone 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 |
|---|
| 67296-1773 | OXYCODONE AND ACETAMINOPHEN TABLET [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 1 package rows | 20220123_a35b801c-cd4a-9595-e053-2a95a90a8baa.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 |
|---|
| 67296-1773-6 | 67296177306 | 6 TABLET in 1 BOTTLE (67296-1773-6) | 6 tablet | 2020-01-01 | 0000-00-00 | No | No | Current |