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Bisoprolol

NDC 42571-470, Bisoprolol Fumarate, tablet, film coated, from Micro Labs Limited.

Product NDC
42571-470
Status
Listed
Labeler
Micro Labs Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218303
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42571-470 \
  -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
42571-470-0142571047001100 TABLET, FILM COATED in 1 BOTTLE (42571-470-01)
42571-470-0542571047005500 TABLET, FILM COATED in 1 BOTTLE (42571-470-05)
42571-470-304257104703030 TABLET, FILM COATED in 1 BOTTLE (42571-470-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c3ee566c-74c4-45f4-a947-526a7313e326

Use it

Look up 42571-470 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42571-470 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42571-470. 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.