hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydroxyzine hydrochloride
Generic Name hydroxyzine hydrochloride
Labeler remedyrepack inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

hydroxyzine dihydrochloride 25 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2066
Product ID 70518-2066_499c7349-9995-6589-e063-6394a90a0e58
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA088618
Listing Expiration 2027-12-31
Marketing Start 2019-05-07

Pharmacologic Class

Classes
antihistamine [epc] histamine receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182066
Hyphenated Format 70518-2066

Supplemental Identifiers

RxCUI
995258
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 ANDA088618 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2066-0)
source: ndc

Packages (1)

70518-2066-0 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2066-0)

Ingredients (1)

hydroxyzine dihydrochloride (25 mg/1)

Linked Drug Pages (1)

Hydroxyzine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "499c7349-9995-6589-e063-6394a90a0e58", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["6ad55cd1-a284-4c3d-aa90-653704afdb75"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2066-0)", "package_ndc": "70518-2066-0", "marketing_start_date": "20190507"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "70518-2066_499c7349-9995-6589-e063-6394a90a0e58", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "70518-2066", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA088618", "marketing_category": "ANDA", "marketing_start_date": "20190507", "listing_expiration_date": "20271231"}