Methocarbamol Tablets, USP, 750 mg
NDC 63561-0174, Methocarbamol, tablet, film coated, from Granulation Technology, Inc..
- Product NDC
- 63561-0174
- Status
- Listed
- Labeler
- Granulation Technology, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA212623
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/63561-0174 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METHOCARBAMOL750 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE]; Muscle Relaxant [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 63561-0174-1 | 63561017401 | 100 TABLET, FILM COATED in 1 BOTTLE (63561-0174-1) |
| 63561-0174-5 | 63561017405 | 500 TABLET, FILM COATED in 1 BOTTLE (63561-0174-5) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/70c5342c-9597-4fe6-863c-f8ae4adc063aNADAC price for package 63561017401
GET /v1/drugs/nadac/63561017401NADAC price for package 63561017405
GET /v1/drugs/nadac/63561017405
Use it
Look up 63561-0174 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/63561-0174 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 63561-0174. 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.