Acetaminophen and Codeine Phosphate
NDC 70518-4104, Acetaminophen and Codeine Phosphate, tablet, from REMEDYREPACK INC..
- Product NDC
- 70518-4104
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA089805
- DEA schedule
- CIII
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4104 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ACETAMINOPHEN300 mg/1
- CODEINE PHOSPHATE30 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA]; Opioid Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-4104-0 | 70518410400 | 30 TABLET in 1 BLISTER PACK (70518-4104-0) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/40d4a71e-341e-48b3-b925-ba35b7910dff
Use it
Look up 70518-4104 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4104 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-4104. 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.