68071-2178 NDC - MECLIZINE HCL 25 MG ()

Drug Information

Product NDC: 68071-2178

Proprietary Name: Meclizine HCl 25 mg

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: NuCare Pharmceuticals,Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/15/2015

Package Information

No. Package Code Package Description Billing Unit
168071-2178-220 TABLET, CHEWABLE in 1 BOTTLE (68071-2178-2)
268071-2178-330 TABLET, CHEWABLE in 1 BOTTLE (68071-2178-3)
368071-2178-440 TABLET, CHEWABLE in 1 BOTTLE (68071-2178-4)
468071-2178-660 TABLET, CHEWABLE in 1 BOTTLE (68071-2178-6)

NDC Record

Field Name Field Value Definition
PRODUCT NDC68071-2178The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEMeclizine HCl 25 mgThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/15/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMENuCare Pharmceuticals,Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023