meclizine hydrochloride

Generic: meclizine hydrochloride

Labeler: jubilant cadista pharmacuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name meclizine hydrochloride
Generic Name meclizine hydrochloride
Labeler jubilant cadista pharmacuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

meclizine hydrochloride 12.5 mg/1

Manufacturer
Jubilant Cadista Pharmacuticals Inc.

Identifiers & Regulatory

Product NDC 59746-122
Product ID 59746-122_ead33f00-e158-464f-953f-ab5a9a391199
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040659
Marketing Start 2010-06-04
Marketing End 2026-10-31

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59746122
Hyphenated Format 59746-122

Supplemental Identifiers

RxCUI
995624 995666
UPC
0359746121068 0359746122065
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 ANDA040659 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (59746-122-06)
  • 1000 TABLET in 1 BOTTLE (59746-122-10)
source: ndc

Packages (2)

59746-122-06 100 TABLET in 1 BOTTLE (59746-122-06) 59746-122-10 1000 TABLET in 1 BOTTLE (59746-122-10)

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": "ead33f00-e158-464f-953f-ab5a9a391199", "openfda": {"upc": ["0359746121068", "0359746122065"], "unii": ["HDP7W44CIO"], "rxcui": ["995624", "995666"], "spl_set_id": ["9350fefc-9c00-182c-c3a9-044d4a40856f"], "manufacturer_name": ["Jubilant Cadista Pharmacuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59746-122-06)", "package_ndc": "59746-122-06", "marketing_end_date": "20261031", "marketing_start_date": "20100604"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (59746-122-10)", "package_ndc": "59746-122-10", "marketing_end_date": "20261031", "marketing_start_date": "20100604"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "59746-122_ead33f00-e158-464f-953f-ab5a9a391199", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "59746-122", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Jubilant Cadista Pharmacuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MECLIZINE HYDROCHLORIDE", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA040659", "marketing_category": "ANDA", "marketing_end_date": "20261031", "marketing_start_date": "20100604"}