hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydroxyzine hydrochloride
Generic Name hydroxyzine hydrochloride
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR
Active Ingredients

hydroxyzine dihydrochloride 25 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1649
Product ID 51662-1649_19869100-35c6-c014-e063-6294a90a4f11
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA087408
Listing Expiration 2026-12-31
Marketing Start 1990-09-30

Pharmacologic Class

Classes
antihistamine [epc] histamine receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621649
Hyphenated Format 51662-1649

Supplemental Identifiers

RxCUI
995270
UNII
76755771U3

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name hydroxyzine hydrochloride (source: ndc)
Generic Name hydroxyzine hydrochloride (source: ndc)
Application Number ANDA087408 (source: ndc)
Routes
INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 25 mg/mL
source: ndc
Packaging
  • 25 POUCH in 1 CASE (51662-1649-3) / 1 VIAL, MULTI-DOSE in 1 POUCH (51662-1649-2) / 10 mL in 1 VIAL, MULTI-DOSE
source: ndc

Packages (1)

51662-1649-3 25 POUCH in 1 CASE (51662-1649-3) / 1 VIAL, MULTI-DOSE in 1 POUCH (51662-1649-2) / 10 mL in 1 VIAL, MULTI-DOSE

Ingredients (1)

hydroxyzine dihydrochloride (25 mg/mL)

Linked Drug Pages (1)

HYDROXYZINE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR"], "spl_id": "19869100-35c6-c014-e063-6294a90a4f11", "openfda": {"unii": ["76755771U3"], "rxcui": ["995270"], "spl_set_id": ["16a63845-6619-293b-e063-6394a90a0a5c"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "25 POUCH in 1 CASE (51662-1649-3)  / 1 VIAL, MULTI-DOSE in 1 POUCH (51662-1649-2)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "51662-1649-3", "marketing_start_date": "19900930"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "51662-1649_19869100-35c6-c014-e063-6294a90a4f11", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "51662-1649", "generic_name": "HYDROXYZINE HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA087408", "marketing_category": "ANDA", "marketing_start_date": "19900930", "listing_expiration_date": "20261231"}