Oxycodone Hydrochloride and Acetaminophen
- Product NDC
- 60760-200
- 11-digit product format
- 607600200
- Labeler code
- 60760
- Product ID
- 60760-200_7b20c416-522e-737a-e053-2991aa0a5709
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA040777
- Marketing category
- ANDA
- Marketing start
- 2009-06-08
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record