meclizine hydrochloride

Generic: meclizine hydrocloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name meclizine hydrochloride
Generic Name meclizine hydrocloride
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

meclizine hydrochloride 25 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-996
Product ID 63187-996_6d44d894-810c-4608-a503-0cc6ff1f965d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040659
Listing Expiration 2026-12-31
Marketing Start 2010-06-04

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187996
Hyphenated Format 63187-996

Supplemental Identifiers

RxCUI
995666
UPC
0363187996208
UNII
HDP7W44CIO

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 hydrocloride (source: ndc)
Application Number ANDA040659 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (63187-996-10)
  • 20 TABLET in 1 BOTTLE (63187-996-20)
  • 30 TABLET in 1 BOTTLE (63187-996-30)
  • 60 TABLET in 1 BOTTLE (63187-996-60)
  • 90 TABLET in 1 BOTTLE (63187-996-90)
source: ndc

Packages (5)

63187-996-10 10 TABLET in 1 BOTTLE (63187-996-10) 63187-996-20 20 TABLET in 1 BOTTLE (63187-996-20) 63187-996-30 30 TABLET in 1 BOTTLE (63187-996-30) 63187-996-60 60 TABLET in 1 BOTTLE (63187-996-60) 63187-996-90 90 TABLET in 1 BOTTLE (63187-996-90)

Ingredients (1)

meclizine hydrochloride (25 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": "6d44d894-810c-4608-a503-0cc6ff1f965d", "openfda": {"upc": ["0363187996208"], "unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["f574e123-8db7-4e3d-a0ee-e4e1f04ff146"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (63187-996-10)", "package_ndc": "63187-996-10", "marketing_start_date": "20200512"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (63187-996-20)", "package_ndc": "63187-996-20", "marketing_start_date": "20180301"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-996-30)", "package_ndc": "63187-996-30", "marketing_start_date": "20190101"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-996-60)", "package_ndc": "63187-996-60", "marketing_start_date": "20220617"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-996-90)", "package_ndc": "63187-996-90", "marketing_start_date": "20220617"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "63187-996_6d44d894-810c-4608-a503-0cc6ff1f965d", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "63187-996", "generic_name": "Meclizine Hydrocloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MECLIZINE HYDROCHLORIDE", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040659", "marketing_category": "ANDA", "marketing_start_date": "20100604", "listing_expiration_date": "20261231"}