Acetaminophen and Codeine Phosphate
- Product NDC
- 60432-245
- 11-digit product format
- 604320245
- Labeler code
- 60432
- Product ID
- 60432-245_5c9c2a4f-49bc-4bba-8507-00844258477c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acetaminophen and codeine phosphate
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Morton Grove Pharmaceuticals, Inc.
- Application
- ANDA087006
- Marketing category
- ANDA
- Marketing start
- 1981-07-22
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; CODEINE PHOSPHATE
- Active strength
- 120 mg/5mL; mg/5mL
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record