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Prazosin Hydrochloride

NDC 68788-8742, Prazosin Hydrochloride, capsule, from Preferred Pharmaceuticals Inc..

Product NDC
68788-8742
Status
Listed
Labeler
Preferred 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/68788-8742 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAZOSIN HYDROCHLORIDE2 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68788-8742-168788874201100 CAPSULE in 1 BOTTLE (68788-8742-1)
68788-8742-36878887420330 CAPSULE in 1 BOTTLE (68788-8742-3)
68788-8742-66878887420660 CAPSULE in 1 BOTTLE (68788-8742-6)
68788-8742-96878887420990 CAPSULE in 1 BOTTLE (68788-8742-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c4449fa8-a637-4780-8e19-51cb54e1ee68

Use it

Look up 68788-8742 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8742 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8742. 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.