Acetaminophen and Codeine Phosphate
NDC 0121-1008, ACETAMINOPHEN and CODEINE PHOSPHATE, solution, from PAI Holdings, LLC dba PAI Pharma.
- Product NDC
- 0121-1008
- Status
- Listed
- Labeler
- PAI Holdings, LLC dba PAI Pharma
- Dosage form
- SOLUTION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA087508
- DEA schedule
- CV
curl https://api.healthcare.dev/v1/drugs/ndc/0121-1008 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ACETAMINOPHEN300 mg/12.5mL
- CODEINE PHOSPHATE30 mg/12.5mL
Pharmacologic classes
Full Opioid Agonists [MoA]; Opioid Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0121-1008-40 | 00121100840 | 40 TRAY in 1 CASE (0121-1008-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 12.5 mL in 1 CUP, UNIT-DOSE (0121-1008-12) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/95ac6875-6b14-4cde-8efb-80704e39b8d8
Use it
Look up 0121-1008 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0121-1008 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0121-1008. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.