meclizine hcl 25 mg
Generic: meclizine hcl
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
meclizine hcl 25 mg
Generic Name
meclizine hcl
Labeler
preferred pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
meclizine hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-7982
Product ID
68788-7982_4fb1109d-7da8-4817-9b36-dae9af321552
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
part336
Listing Expiration
2026-12-31
Marketing Start
2021-07-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687887982
Hyphenated Format
68788-7982
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 hcl 25 mg (source: ndc)
Generic Name
meclizine hcl (source: ndc)
Application Number
part336 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 10 TABLET in 1 BOTTLE, PLASTIC (68788-7982-1)
- 30 TABLET in 1 BOTTLE, PLASTIC (68788-7982-3)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4fb1109d-7da8-4817-9b36-dae9af321552", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995632"], "spl_set_id": ["e4201bdc-18b4-4229-a7c0-300c5d5ad8db"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (68788-7982-1)", "package_ndc": "68788-7982-1", "marketing_start_date": "20210728"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (68788-7982-3)", "package_ndc": "68788-7982-3", "marketing_start_date": "20210728"}], "brand_name": "Meclizine HCL 25 mg", "product_id": "68788-7982_4fb1109d-7da8-4817-9b36-dae9af321552", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "68788-7982", "generic_name": "Meclizine HCL", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Meclizine HCL 25 mg", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "part336", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210728", "listing_expiration_date": "20261231"}