meclizine hydrochloride
Generic: meclizine hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
meclizine hydrochloride
Generic Name
meclizine hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
meclizine hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-1825
Product ID
71335-1825_e1e6f9e4-9b01-4878-86ee-fc6c38b61932
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA010721
Listing Expiration
2026-12-31
Marketing Start
2020-01-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713351825
Hyphenated Format
71335-1825
Supplemental Identifiers
RxCUI
UNII
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
NDA010721 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 14 TABLET in 1 BOTTLE (71335-1825-0)
- 90 TABLET in 1 BOTTLE (71335-1825-1)
- 30 TABLET in 1 BOTTLE (71335-1825-2)
- 25 TABLET in 1 BOTTLE (71335-1825-3)
- 20 TABLET in 1 BOTTLE (71335-1825-4)
- 40 TABLET in 1 BOTTLE (71335-1825-5)
- 60 TABLET in 1 BOTTLE (71335-1825-6)
- 120 TABLET in 1 BOTTLE (71335-1825-7)
- 10 TABLET in 1 BOTTLE (71335-1825-8)
- 100 TABLET in 1 BOTTLE (71335-1825-9)
Packages (10)
71335-1825-0
14 TABLET in 1 BOTTLE (71335-1825-0)
71335-1825-1
90 TABLET in 1 BOTTLE (71335-1825-1)
71335-1825-2
30 TABLET in 1 BOTTLE (71335-1825-2)
71335-1825-3
25 TABLET in 1 BOTTLE (71335-1825-3)
71335-1825-4
20 TABLET in 1 BOTTLE (71335-1825-4)
71335-1825-5
40 TABLET in 1 BOTTLE (71335-1825-5)
71335-1825-6
60 TABLET in 1 BOTTLE (71335-1825-6)
71335-1825-7
120 TABLET in 1 BOTTLE (71335-1825-7)
71335-1825-8
10 TABLET in 1 BOTTLE (71335-1825-8)
71335-1825-9
100 TABLET in 1 BOTTLE (71335-1825-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e1e6f9e4-9b01-4878-86ee-fc6c38b61932", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["27b6a7e0-a361-4705-9f31-719063a65f22"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE (71335-1825-0)", "package_ndc": "71335-1825-0", "marketing_start_date": "20220224"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1825-1)", "package_ndc": "71335-1825-1", "marketing_start_date": "20220224"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1825-2)", "package_ndc": "71335-1825-2", "marketing_start_date": "20220224"}, {"sample": false, "description": "25 TABLET in 1 BOTTLE (71335-1825-3)", "package_ndc": "71335-1825-3", "marketing_start_date": "20220224"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-1825-4)", "package_ndc": "71335-1825-4", "marketing_start_date": "20220224"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-1825-5)", "package_ndc": "71335-1825-5", "marketing_start_date": "20220224"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1825-6)", "package_ndc": "71335-1825-6", "marketing_start_date": "20220224"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-1825-7)", "package_ndc": "71335-1825-7", "marketing_start_date": "20220224"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-1825-8)", "package_ndc": "71335-1825-8", "marketing_start_date": "20220224"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1825-9)", "package_ndc": "71335-1825-9", "marketing_start_date": "20220224"}], "brand_name": "Meclizine Hydrochloride", "product_id": "71335-1825_e1e6f9e4-9b01-4878-86ee-fc6c38b61932", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "71335-1825", "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": "25 mg/1"}], "application_number": "NDA010721", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200115", "listing_expiration_date": "20261231"}