Oxycodone and Acetaminophen
- Product NDC
- 68071-4839
- 11-digit product format
- 680714839
- Labeler code
- 68071
- Product ID
- 68071-4839_bb901651-d4a6-f6e6-e053-2a95a90ab6ee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA207419
- Marketing category
- ANDA
- Marketing start
- 2017-04-11
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN
- Active strength
- 5 mg/1; mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 68071-4839-6 | 68071483906 | 6 TABLET in 1 BOTTLE (68071-4839-6) | 6 tablet | 2019-04-09 | 0000-00-00 | No | No | Current |