ACETAMINOPHEN AND CODEINE PHOSPHATE
NDC 72162-2001, acetaminophen and codeine phosphate, tablet, from Bryant Ranch Prepack.
- Product NDC
- 72162-2001
- 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/72162-2001 \ -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 |
|---|---|---|
| 72162-2001-1 | 72162200101 | 100 TABLET in 1 BOTTLE (72162-2001-1) |
| 72162-2001-5 | 72162200105 | 500 TABLET in 1 BOTTLE (72162-2001-5) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/879db1b5-6365-4151-9879-80d8a2a3cd8a
Use it
Look up 72162-2001 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2001 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72162-2001. 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.