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Olmesartan Medoxomil

NDC 46708-133, Olmesartan Medoxomil, tablet, film coated, from Alembic Pharmaceuticals Limited.

Product NDC
46708-133
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203012
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-133 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OLMESARTAN MEDOXOMIL40 mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA]; Angiotensin 2 Receptor Blocker [EPC]

Package NDCNDC-11Package
46708-133-1046708013310100 TABLET, FILM COATED in 1 CARTON (46708-133-10)
46708-133-304670801333030 TABLET, FILM COATED in 1 BOTTLE (46708-133-30)
46708-133-904670801339090 TABLET, FILM COATED in 1 BOTTLE (46708-133-90)
46708-133-91467080133911000 TABLET, FILM COATED in 1 BOTTLE (46708-133-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ac08ea7d-f529-42ca-850a-a0ecce7dc830

Use it

Look up 46708-133 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-133 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-133. 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.