meclizine hydrochloride

Generic: meclizine hydrocloride

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

meclizine hydrochloride 25 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-3017
Product ID 68071-3017_1d788e6f-633a-a344-e063-6294a90a90d1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040659
Listing Expiration 2026-12-31
Marketing Start 2010-06-04

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713017
Hyphenated Format 68071-3017

Supplemental Identifiers

RxCUI
995666
UPC
0368071301731
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
  • 12 TABLET in 1 BOTTLE (68071-3017-1)
  • 20 TABLET in 1 BOTTLE (68071-3017-2)
  • 30 TABLET in 1 BOTTLE (68071-3017-3)
  • 60 TABLET in 1 BOTTLE (68071-3017-6)
  • 10 TABLET in 1 BOTTLE (68071-3017-7)
  • 90 TABLET in 1 BOTTLE (68071-3017-9)
source: ndc

Packages (6)

68071-3017-1 12 TABLET in 1 BOTTLE (68071-3017-1) 68071-3017-2 20 TABLET in 1 BOTTLE (68071-3017-2) 68071-3017-3 30 TABLET in 1 BOTTLE (68071-3017-3) 68071-3017-6 60 TABLET in 1 BOTTLE (68071-3017-6) 68071-3017-7 10 TABLET in 1 BOTTLE (68071-3017-7) 68071-3017-9 90 TABLET in 1 BOTTLE (68071-3017-9)

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": "1d788e6f-633a-a344-e063-6294a90a90d1", "openfda": {"upc": ["0368071301731"], "unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["64a508ae-768a-2fba-e053-2991aa0ac42d"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE (68071-3017-1)", "package_ndc": "68071-3017-1", "marketing_start_date": "20180207"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-3017-2)", "package_ndc": "68071-3017-2", "marketing_start_date": "20180207"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3017-3)", "package_ndc": "68071-3017-3", "marketing_start_date": "20180207"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3017-6)", "package_ndc": "68071-3017-6", "marketing_start_date": "20180207"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (68071-3017-7)", "package_ndc": "68071-3017-7", "marketing_start_date": "20180207"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3017-9)", "package_ndc": "68071-3017-9", "marketing_start_date": "20180207"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "68071-3017_1d788e6f-633a-a344-e063-6294a90a90d1", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "68071-3017", "generic_name": "Meclizine Hydrocloride", "labeler_name": "NuCare Pharmaceuticals,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_start_date": "20100604", "listing_expiration_date": "20261231"}