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MEPROBAMATE

NDC 46708-020, MEPROBAMATE, tablet, from Alembic Pharmaceuticals Limited.

Product NDC
46708-020
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090122
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-020 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MEPROBAMATE400 mg/1
Package NDCNDC-11Package
46708-020-304670800203030 TABLET in 1 BOTTLE (46708-020-30)
46708-020-7146708002071100 TABLET in 1 BOTTLE (46708-020-71)
46708-020-91467080020911000 TABLET in 1 BOTTLE (46708-020-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a0891a32-105b-48bc-a246-5e179d2e7fa1

Use it

Look up 46708-020 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-020 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-020. 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.