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HYDROXYZINE HYDROCHLORIDE

NDC 70518-4170, hydroxyzine hydrochloride, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-4170
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/70518-4170 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROXYZINE HYDROCHLORIDE50 mg/1

Pharmacologic classes

Antihistamine [EPC]; Histamine Receptor Antagonists [MoA]

Package NDCNDC-11Package
70518-4170-07051841700030 TABLET, FILM COATED in 1 BLISTER PACK (70518-4170-0)
70518-4170-17051841700190 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-1)
70518-4170-27051841700230 TABLET, FILM COATED in 1 BLISTER PACK (70518-4170-2)
70518-4170-37051841700360 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-3)
70518-4170-47051841700490 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-4)
70518-4170-57051841700530 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-5)
70518-4170-67051841700660 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f6ad4729-b291-42c4-8483-99385d8043db

Use it

Look up 70518-4170 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4170 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4170. 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.