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HYDROXYZINE HYDROCHLORIDE

NDC 10135-810, hydroxyzine hydrochloride, tablet, film coated, from Marlex Pharmaceuticals, Inc..

Product NDC
10135-810
Status
Listed
Labeler
Marlex Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207121
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10135-810 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROXYZINE DIHYDROCHLORIDE10 mg/1

Pharmacologic classes

Antihistamine [EPC]; Histamine Receptor Antagonists [MoA]

Package NDCNDC-11Package
10135-810-0110135081001100 TABLET, FILM COATED in 1 BOTTLE (10135-810-01)
10135-810-10101350810101000 TABLET, FILM COATED in 1 BOTTLE (10135-810-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/31a907e6-7fae-0682-e063-6294a90a24a5

Use it

Look up 10135-810 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10135-810 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10135-810. 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.