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HYDROXYZINE HYDROCHLORIDE

NDC 68788-8872, hydroxyzine hydrochloride, tablet, film coated, from Preferred Pharmaceuticals Inc..

Product NDC
68788-8872
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217652
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8872 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROXYZINE HYDROCHLORIDE10 mg/1

Pharmacologic classes

Antihistamine [EPC]; Histamine Receptor Antagonists [MoA]

Package NDCNDC-11Package
68788-8872-36878888720330 TABLET, FILM COATED in 1 BOTTLE (68788-8872-3)
68788-8872-56878888720560 TABLET, FILM COATED in 1 BOTTLE (68788-8872-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a35d1fe2-328d-42ff-ba1f-18a7f2f03c88

Use it

Look up 68788-8872 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8872 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8872. 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.