meclizine hydrochloride
Generic: meclizine
Labeler: ncs healthcare of ky, llc dba vangard labsDrug Facts
Product Profile
Brand Name
meclizine hydrochloride
Generic Name
meclizine
Labeler
ncs healthcare of ky, llc dba vangard labs
Dosage Form
TABLET
Routes
Active Ingredients
meclizine hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0615-8515
Product ID
0615-8515_7c702061-6604-4b46-b035-dd0fb4d25165
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202640
Listing Expiration
2026-12-31
Marketing Start
2023-09-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
06158515
Hyphenated Format
0615-8515
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 (source: ndc)
Application Number
ANDA202640 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 30 TABLET in 1 BLISTER PACK (0615-8515-39)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7c702061-6604-4b46-b035-dd0fb4d25165", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624", "995666"], "spl_set_id": ["1a33dec1-8d59-48bd-aaef-77d162194d57"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-8515-39)", "package_ndc": "0615-8515-39", "marketing_start_date": "20240716"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "0615-8515_7c702061-6604-4b46-b035-dd0fb4d25165", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "0615-8515", "generic_name": "MECLIZINE", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MECLIZINE HYDROCHLORIDE", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA202640", "marketing_category": "ANDA", "marketing_start_date": "20230914", "listing_expiration_date": "20261231"}