meclizine hydrochloride
Generic: meclizine hydrocloride
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
meclizine hydrochloride
Generic Name
meclizine hydrocloride
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
meclizine hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-1308
Product ID
70518-1308_48d4b741-6e96-0343-e063-6294a90a427e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040659
Marketing Start
2018-08-17
Marketing End
2026-10-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705181308
Hyphenated Format
70518-1308
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 hydrocloride (source: ndc)
Application Number
ANDA040659 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 90 TABLET in 1 BOTTLE, PLASTIC (70518-1308-0)
- 10 TABLET in 1 BOTTLE, PLASTIC (70518-1308-5)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48d4b741-6e96-0343-e063-6294a90a427e", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["ba2fb6de-af86-4c05-9018-135e1f8594f9"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-1308-0)", "package_ndc": "70518-1308-0", "marketing_end_date": "20261031", "marketing_start_date": "20180817"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (70518-1308-5)", "package_ndc": "70518-1308-5", "marketing_end_date": "20261031", "marketing_start_date": "20231218"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "70518-1308_48d4b741-6e96-0343-e063-6294a90a427e", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "70518-1308", "generic_name": "Meclizine Hydrocloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MECLIZINE HYDROCHLORIDE", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040659", "marketing_category": "ANDA", "marketing_end_date": "20261031", "marketing_start_date": "20180817"}