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tamsulosin hydrochloride

NDC 0781-2076, tamsulosin hydrochloride, capsule, from Sandoz Inc.

Product NDC
0781-2076
Status
Listed
Labeler
Sandoz Inc
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078015
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0781-2076 \
  -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
0781-2076-0100781207601100 CAPSULE in 1 BOTTLE (0781-2076-01)
0781-2076-10007812076101000 CAPSULE in 1 BOTTLE (0781-2076-10)
0781-2076-920078120769290 CAPSULE in 1 BOTTLE (0781-2076-92)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fb120098-b007-4a33-80b8-b7279c7668ee

Use it

Look up 0781-2076 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0781-2076 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0781-2076. 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.