Acetaminophen and Codeine Phosphate
- Product NDC
- 51079-161
- 11-digit product format
- 510790161
- Labeler code
- 51079
- Product ID
- 51079-161_938ffe10-4477-a1e4-e053-2a95a90a3508
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acetaminophen and Codeine Phosphate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA088628
- Marketing category
- ANDA
- Marketing start
- 1996-12-23
- Marketing end
- 2021-01-31
- Substance
- ACETAMINOPHEN; CODEINE PHOSPHATE
- Active strength
- 300 mg/1; mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record