Primlev
- Product NDC
- 24090-683
- 11-digit product format
- 240900683
- Labeler code
- 24090
- Product ID
- 24090-683_a3e037f0-fa7c-ba94-e053-2a95a90ab250
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxycodone and acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Akrimax Pharmaceuticals, LLC
- Application
- ANDA040608
- Marketing category
- ANDA
- Marketing start
- 2011-12-01
- Marketing end
- 2020-12-01
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record