Oxycodone and Acetaminophen
- Product NDC
- 60760-276
- 11-digit product format
- 607600276
- Labeler code
- 60760
- Product ID
- 60760-276_7b20c416-51de-737a-e053-2991aa0a5709
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA201972
- Marketing category
- ANDA
- Marketing start
- 2013-07-15
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN
- Active strength
- 10 mg/1; mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 60760-276-30 | 60760027630 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-276-30) | 30 tablet | 2017-12-15 | 0000-00-00 | No | No | Current |
| 60760-276-60 | 60760027660 | 60 TABLET in 1 BOTTLE, PLASTIC (60760-276-60) | 60 tablet | 2017-12-15 | 0000-00-00 | No | No | Current |
| 60760-276-90 | 60760027690 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-276-90) | 90 tablet | 2017-12-15 | 0000-00-00 | No | No | Current |