meclizine hydrochloride
Generic: meclizine hydrochloride
Labeler: cvs pharmacy, incDrug Facts
Product Profile
Brand Name
meclizine hydrochloride
Generic Name
meclizine hydrochloride
Labeler
cvs pharmacy, inc
Dosage Form
TABLET
Routes
Active Ingredients
meclizine hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69842-857
Product ID
69842-857_41499ece-5964-999d-e063-6394a90ab8fb
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M009
Listing Expiration
2026-12-31
Marketing Start
2020-08-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69842857
Hyphenated Format
69842-857
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
M009 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 2 BLISTER PACK in 1 CARTON (69842-857-05) / 8 TABLET in 1 BLISTER PACK
- 1 VIAL in 1 CARTON (69842-857-09) / 8 TABLET in 1 VIAL
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41499ece-5964-999d-e063-6394a90ab8fb", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["b57fc6c2-fbfc-24c3-e053-2995a90a3389"], "manufacturer_name": ["CVS Pharmacy, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (69842-857-05) / 8 TABLET in 1 BLISTER PACK", "package_ndc": "69842-857-05", "marketing_start_date": "20201028"}, {"sample": false, "description": "1 VIAL in 1 CARTON (69842-857-09) / 8 TABLET in 1 VIAL", "package_ndc": "69842-857-09", "marketing_start_date": "20200813"}], "brand_name": "Meclizine Hydrochloride", "product_id": "69842-857_41499ece-5964-999d-e063-6394a90ab8fb", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "69842-857", "generic_name": "Meclizine Hydrochloride", "labeler_name": "CVS Pharmacy, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200813", "listing_expiration_date": "20261231"}