Methocarbamol
NDC 72789-110, Methocarbamol, tablet, film coated, from PD-Rx Pharmaceuticals, Inc..
- Product NDC
- 72789-110
- Status
- Listed
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA208507
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72789-110 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METHOCARBAMOL500 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE]; Muscle Relaxant [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72789-110-40 | 72789011040 | 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-110-40) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/12c8da39-3a0e-4303-9655-29dd83507837
Use it
Look up 72789-110 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72789-110 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72789-110. 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.