methocarbamol
NDC 72887-873, methocarbamol, tablet, film coated, from FH2 PHARMA LLC.
- Product NDC
- 72887-873
- Status
- Listed
- Labeler
- FH2 PHARMA LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA212707
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72887-873 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METHOCARBAMOL1000 mg/1
Pharmacologic classes
Centrally-mediated Muscle Relaxation [PE]; Muscle Relaxant [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72887-873-03 | 72887087303 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72887-873-03) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/1dd56e3d-7ca7-1443-e063-6294a90a13c5
Use it
Look up 72887-873 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72887-873 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72887-873. 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.