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HYDROXYZINE HYDROCHLORIDE

NDC 70518-4141, hydroxyzine hydrochloride, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-4141
Status
Listed
Labeler
REMEDYREPACK 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/70518-4141 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROXYZINE HYDROCHLORIDE25 mg/1

Pharmacologic classes

Antihistamine [EPC]; Histamine Receptor Antagonists [MoA]

Package NDCNDC-11Package
70518-4141-07051841410030 TABLET, FILM COATED in 1 BLISTER PACK (70518-4141-0)
70518-4141-17051841410130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4141-1)
70518-4141-27051841410290 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4141-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8f41912e-12ce-4174-a0fb-cfb4888d8d58

Use it

Look up 70518-4141 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4141 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4141. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.