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Prazosin hydrochloride

NDC 70518-3928, Prazosin hydrochloride, capsule, from REMEDYREPACK INC..

Product NDC
70518-3928
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213406
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3928 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAZOSIN HYDROCHLORIDE1 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70518-3928-07051839280030 CAPSULE in 1 BLISTER PACK (70518-3928-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/960f4d8d-6683-44ff-a3a7-e0f922e621b9

Use it

Look up 70518-3928 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3928 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3928. 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.