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Pindolol

NDC 57664-656, Pindolol, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
57664-656
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074063
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57664-656 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PINDOLOL10 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]

Package NDCNDC-11Package
57664-656-8857664065688100 TABLET in 1 BOTTLE, PLASTIC (57664-656-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b331a73f-bf7b-4442-8901-36d016530279

  • NADAC price for package 57664065688

    GET /v1/drugs/nadac/57664065688

Use it

Look up 57664-656 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57664-656 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57664-656. 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.