Oxycodone and Acetaminophen
- Product NDC
- 63629-7824
- 11-digit product format
- 636297824
- Labeler code
- 63629
- Product ID
- 63629-7824_3cd81d92-7a23-41ec-ab28-ec15e84b2600
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202677
- Marketing category
- ANDA
- Marketing start
- 2016-03-09
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7824-1 | 63629782401 | 21 TABLET in 1 BOTTLE (63629-7824-1) | 21 tablet | 2016-07-25 | 0000-00-00 | No | No | Current |