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NDC 0078-0489, amlodipine besylate and valsartan, tablet, film coated, from Novartis Pharmaceuticals Corporation.

Product NDC
0078-0489
Status
Listed
Labeler
Novartis Pharmaceuticals Corporation
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA021990
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0078-0489 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMLODIPINE BESYLATE10 mg/1
  • VALSARTAN160 mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA]; Angiotensin 2 Receptor Blocker [EPC]; Calcium Channel Antagonists [MoA]; Calcium Channel Blocker [EPC]; Cytochrome P450 3A Inhibitors [MoA]; Dihydropyridine Calcium Channel Blocker [EPC]; Dihydropyridines [CS]

Package NDCNDC-11Package
0078-0489-150007804891530 TABLET, FILM COATED in 1 BOTTLE (0078-0489-15)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d0caec89-96ec-411d-a933-63eda74a6da7

Use it

Look up 0078-0489 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0078-0489 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0078-0489. 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.