meclizine hydrochloride

Generic: meclizine hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name meclizine hydrochloride
Generic Name meclizine hydrochloride
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

meclizine hydrochloride 25 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3815
Product ID 70518-3815_4b1e6b60-d86e-de46-e063-6294a90aa3a7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA010721
Listing Expiration 2027-12-31
Marketing Start 2023-08-02

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183815
Hyphenated Format 70518-3815

Supplemental Identifiers

RxCUI
995666
UNII
HDP7W44CIO

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (70518-3815-1)
  • 30 TABLET in 1 BLISTER PACK (70518-3815-2)
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-3815-3)
  • 30 TABLET in 1 BOTTLE, PLASTIC (70518-3815-4)
  • 10 TABLET in 1 BOTTLE, PLASTIC (70518-3815-5)
source: ndc

Packages (5)

70518-3815-1 30 TABLET in 1 BOTTLE, PLASTIC (70518-3815-1) 70518-3815-2 30 TABLET in 1 BLISTER PACK (70518-3815-2) 70518-3815-3 90 TABLET in 1 BOTTLE, PLASTIC (70518-3815-3) 70518-3815-4 30 TABLET in 1 BOTTLE, PLASTIC (70518-3815-4) 70518-3815-5 10 TABLET in 1 BOTTLE, PLASTIC (70518-3815-5)

Ingredients (1)

meclizine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Meclizine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4b1e6b60-d86e-de46-e063-6294a90aa3a7", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["21d4a6ee-0a66-45d7-bab9-c5eef399713d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-3815-1)", "package_ndc": "70518-3815-1", "marketing_start_date": "20240406"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3815-2)", "package_ndc": "70518-3815-2", "marketing_start_date": "20250207"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-3815-3)", "package_ndc": "70518-3815-3", "marketing_start_date": "20250913"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-3815-4)", "package_ndc": "70518-3815-4", "marketing_start_date": "20260112"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (70518-3815-5)", "package_ndc": "70518-3815-5", "marketing_start_date": "20260217"}], "brand_name": "Meclizine Hydrochloride", "product_id": "70518-3815_4b1e6b60-d86e-de46-e063-6294a90aa3a7", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "70518-3815", "generic_name": "Meclizine Hydrochloride", "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": "NDA010721", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20230802", "listing_expiration_date": "20271231"}