ACETAMINOPHEN AND CODEINE PHOSPHATE
NDC 72162-2002, acetaminophen and codeine phosphate, tablet, from Bryant Ranch Prepack.
- Product NDC
- 72162-2002
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA211610
- DEA schedule
- CIII
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2002 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ACETAMINOPHEN300 mg/1
- CODEINE PHOSPHATE60 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA]; Opioid Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72162-2002-1 | 72162200201 | 100 TABLET in 1 BOTTLE (72162-2002-1) |
| 72162-2002-5 | 72162200205 | 500 TABLET in 1 BOTTLE (72162-2002-5) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/e73b17c4-9f24-4b32-8920-61c58c40a714
Use it
Look up 72162-2002 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2002 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72162-2002. 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.