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Amlodipine and Atorvastatin

NDC 62332-757, Amlodipine and Atorvastatin, tablet, film coated, from Alembic Pharmaceuticals Inc..

Product NDC
62332-757
Status
Listed
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217279
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62332-757 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMLODIPINE BESYLATE2.5 mg/1
  • ATORVASTATIN CALCIUM TRIHYDRATE40 mg/1

Pharmacologic classes

Calcium Channel Antagonists [MoA]; Calcium Channel Blocker [EPC]; Cytochrome P450 3A Inhibitors [MoA]; Dihydropyridine Calcium Channel Blocker [EPC]; Dihydropyridines [CS]; HMG-CoA Reductase Inhibitor [EPC]; Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Package NDCNDC-11Package
62332-757-306233207573030 TABLET, FILM COATED in 1 BOTTLE (62332-757-30)
62332-757-906233207579090 TABLET, FILM COATED in 1 BOTTLE (62332-757-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1346631f-e6db-4c5c-a6af-5aa7b80a011d

  • NADAC price for package 62332075730

    GET /v1/drugs/nadac/62332075730

Use it

Look up 62332-757 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62332-757 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62332-757. 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.