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Dutasteride and tamsulosin hydrochloride

NDC 70771-1356, Dutasteride and tamsulosin hydrochloride, capsule, from Zydus Lifesciences Limited.

Product NDC
70771-1356
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207769
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1356 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DUTASTERIDE.5 mg/1
  • TAMSULOSIN HYDROCHLORIDE.4 mg/1

Pharmacologic classes

5-alpha Reductase Inhibitor [EPC]; 5-alpha Reductase Inhibitors [MoA]; Adrenergic alpha-Antagonists [MoA]; alpha-Adrenergic Blocker [EPC]

Package NDCNDC-11Package
70771-1356-37077113560330 CAPSULE in 1 BOTTLE (70771-1356-3)
70771-1356-97077113560990 CAPSULE in 1 BOTTLE (70771-1356-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4b89b07e-9d19-47a2-bd53-bc5eef9deed1

Use it

Look up 70771-1356 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1356 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1356. 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.