meclizine hydrochloride

Generic: meclizine hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name meclizine hydrochloride
Generic Name meclizine hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

meclizine hydrochloride 12.5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1563
Product ID 71335-1563_7e501fc0-081b-4e64-b2fd-e2193ddb55b6
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 713351563
Hyphenated Format 71335-1563

Supplemental Identifiers

RxCUI
995624
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 hydrochloride (source: ndc)
Application Number ANDA040659 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1563-1)
  • 60 TABLET in 1 BOTTLE (71335-1563-2)
  • 90 TABLET in 1 BOTTLE (71335-1563-3)
  • 28 TABLET in 1 BOTTLE (71335-1563-4)
  • 20 TABLET in 1 BOTTLE (71335-1563-5)
  • 120 TABLET in 1 BOTTLE (71335-1563-6)
  • 100 TABLET in 1 BOTTLE (71335-1563-7)
source: ndc

Packages (7)

71335-1563-1 30 TABLET in 1 BOTTLE (71335-1563-1) 71335-1563-2 60 TABLET in 1 BOTTLE (71335-1563-2) 71335-1563-3 90 TABLET in 1 BOTTLE (71335-1563-3) 71335-1563-4 28 TABLET in 1 BOTTLE (71335-1563-4) 71335-1563-5 20 TABLET in 1 BOTTLE (71335-1563-5) 71335-1563-6 120 TABLET in 1 BOTTLE (71335-1563-6) 71335-1563-7 100 TABLET in 1 BOTTLE (71335-1563-7)

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": "7e501fc0-081b-4e64-b2fd-e2193ddb55b6", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624"], "spl_set_id": ["53f410fd-104c-42c1-9740-6f48ffbc974f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1563-1)", "package_ndc": "71335-1563-1", "marketing_start_date": "20100604"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1563-2)", "package_ndc": "71335-1563-2", "marketing_start_date": "20100604"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1563-3)", "package_ndc": "71335-1563-3", "marketing_start_date": "20100604"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-1563-4)", "package_ndc": "71335-1563-4", "marketing_start_date": "20100604"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-1563-5)", "package_ndc": "71335-1563-5", "marketing_start_date": "20100604"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-1563-6)", "package_ndc": "71335-1563-6", "marketing_start_date": "20100604"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1563-7)", "package_ndc": "71335-1563-7", "marketing_start_date": "20100604"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "71335-1563_7e501fc0-081b-4e64-b2fd-e2193ddb55b6", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "71335-1563", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "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_start_date": "20100604", "listing_expiration_date": "20261231"}