meclizine hydrochloride

Generic: meclizine hydrocloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

meclizine hydrochloride 25 mg/1

Manufacturer
REMEDYREPACK INC.

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
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705181308
Hyphenated Format 70518-1308

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 hydrocloride (source: ndc)
Application Number ANDA040659 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-1308-0)
  • 10 TABLET in 1 BOTTLE, PLASTIC (70518-1308-5)
source: ndc

Packages (2)

Ingredients (1)

meclizine hydrochloride (25 mg/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"}