Oxycodone and Acetaminophen
- Product NDC
- 0527-1669
- 11-digit product format
- 005271669
- Labeler code
- 0527
- Product ID
- 0527-1669_280e762b-67ec-41a6-b1ef-1d99a09f787e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA207333
- Marketing category
- ANDA
- Marketing start
- 2017-09-25
- 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 |
|---|
| 0527-1669-01 | 00527166901 | 100 TABLET in 1 BOTTLE (0527-1669-01) | 100 tablet | 2017-09-25 | 0000-00-00 | No | No | Current |
| 0527-1669-05 | 00527166905 | 500 TABLET in 1 BOTTLE (0527-1669-05) | 500 tablet | 2017-09-25 | 0000-00-00 | No | No | Current |