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NDC 0037-2250, Carisoprodol, tablet, from Viatris Specialty LLC.

Product NDC
0037-2250
Status
Listed
Labeler
Viatris Specialty LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA011792
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0037-2250 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CARISOPRODOL250 mg/1

Pharmacologic classes

Centrally-mediated Muscle Relaxation [PE]; Muscle Relaxant [EPC]

Package NDCNDC-11Package
0037-2250-1000037225010100 TABLET in 1 BOTTLE, PLASTIC (0037-2250-10)
0037-2250-300003722503030 TABLET in 1 BOTTLE, PLASTIC (0037-2250-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6297cf20-830a-11dc-94c8-0002a5d5c51b

Use it

Look up 0037-2250 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0037-2250 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0037-2250. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.