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BISOPROLOL FUMARATE

NDC 70095-020, BISOPROLOL FUMARATE, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
70095-020
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217617
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70095-020 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BISOPROLOL FUMARATE5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70095-020-017009500200130 TABLET, FILM COATED in 1 BOTTLE, UNIT-DOSE (70095-020-01)
70095-020-0270095002002100 TABLET, FILM COATED in 1 BOTTLE (70095-020-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7556f457-c4d3-49d6-b383-0ade6d489091

  • NADAC price for package 70095002001

    GET /v1/drugs/nadac/70095002001

  • NADAC price for package 70095002002

    GET /v1/drugs/nadac/70095002002

Use it

Look up 70095-020 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70095-020 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70095-020. 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.