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Tamsulosin Hydrochloride

NDC 70518-0179, Tamsulosin Hydrochloride, capsule, from REMEDYREPACK INC..

Product NDC
70518-0179
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202433
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-0179 \
  -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
70518-0179-370518017903100 POUCH in 1 BOX (70518-0179-3) / 1 CAPSULE in 1 POUCH (70518-0179-4)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b30e2bde-b20e-4899-a100-f44170d8165b

Use it

Look up 70518-0179 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-0179 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-0179. 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.