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Tamsulosin hydrochloride

NDC 63672-0021, tamsulosin hydrochloride, capsule, from Synthon Pharmaceuticals, Inc..

Product NDC
63672-0021
Status
Listed
Labeler
Synthon Pharmaceuticals, Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078801
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63672-0021 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TAMSULOSIN HYDROCHLORIDE.4 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
63672-0021-96367200210920000 CAPSULE in 1 DRUM (63672-0021-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/13a5032d-0be1-4001-916e-459f0b1a051d

Use it

Look up 63672-0021 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63672-0021 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63672-0021. 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.