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Prazosin Hydrochloride

NDC 10135-666, Prazosin Hydrochloride, capsule, from Marlex Pharmaceuticals Inc.

Product NDC
10135-666
Status
Listed
Labeler
Marlex Pharmaceuticals Inc
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210971
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10135-666 \
  -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
10135-666-0110135066601100 CAPSULE in 1 BOTTLE (10135-666-01)
10135-666-10101350666101000 CAPSULE in 1 BOTTLE (10135-666-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1c28c337-6dbb-46bd-aa86-dbcd34e3f6e6

Use it

Look up 10135-666 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10135-666 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10135-666. 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.