meclizine hydrochloride

Generic: meclizine hydrochloride

Labeler: epic pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name meclizine hydrochloride
Generic Name meclizine hydrochloride
Labeler epic pharma llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

meclizine hydrochloride 12.5 mg/1

Manufacturer
Epic Pharma LLC

Identifiers & Regulatory

Product NDC 42806-012
Product ID 42806-012_42600718-075b-481b-8fec-cb6cbadab7de
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200294
Listing Expiration 2026-12-31
Marketing Start 2012-04-30

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42806012
Hyphenated Format 42806-012

Supplemental Identifiers

RxCUI
995624 995666
UNII
HDP7W44CIO

Packaging Origin

Original Packager
true

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 meclizine hydrochloride (source: ndc)
Generic Name meclizine hydrochloride (source: ndc)
Application Number ANDA200294 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (42806-012-01)
  • 1000 TABLET in 1 BOTTLE (42806-012-10)
source: ndc

Packages (2)

42806-012-01 100 TABLET in 1 BOTTLE (42806-012-01) 42806-012-10 1000 TABLET in 1 BOTTLE (42806-012-10)

Ingredients (1)

meclizine hydrochloride (12.5 mg/1)

Linked Drug Pages (1)

Meclizine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "42600718-075b-481b-8fec-cb6cbadab7de", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624", "995666"], "spl_set_id": ["467e464b-bbaf-4053-9136-39e47a92fa05"], "manufacturer_name": ["Epic Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42806-012-01)", "package_ndc": "42806-012-01", "marketing_start_date": "20120430"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (42806-012-10)", "package_ndc": "42806-012-10", "marketing_start_date": "20120430"}], "brand_name": "Meclizine Hydrochloride", "product_id": "42806-012_42600718-075b-481b-8fec-cb6cbadab7de", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "42806-012", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Epic Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA200294", "marketing_category": "ANDA", "marketing_start_date": "20120430", "listing_expiration_date": "20261231"}