Morphine sulfate
NDC 72162-1792, morphine sulfate, tablet, film coated, extended release, from Bryant Ranch Prepack.
- Product NDC
- 72162-1792
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA078761
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1792 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MORPHINE SULFATE200 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA]; Opioid Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72162-1792-1 | 72162179201 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1792-1) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/9a1ca529-8268-4be3-b03f-b2f2238cc9dc
Use it
Look up 72162-1792 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1792 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72162-1792. 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.