47682-088 NDC - MEDIQUE ALCALAK ()

Drug Information

  • Product NDC: 47682-088
  • Proprietary Name: Medique Alcalak
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Unifirst First Aid Corporation
Product Type:
FDA Application Number: part331
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:12/30/2008

Package Information

No. Package Code Package Description Billing Unit
147682-088-13250 PACKET in 1 BOX (47682-088-13) / 2 TABLET, CHEWABLE in 1 PACKET
247682-088-3350 PACKET in 1 BOX (47682-088-33) / 2 TABLET, CHEWABLE in 1 PACKET
347682-088-47100 PACKET in 1 BOX (47682-088-47) / 2 TABLET, CHEWABLE in 1 PACKET (47682-088-99)
447682-088-6412 PACKET in 1 BOX (47682-088-64) / 2 TABLET, CHEWABLE in 1 PACKET
547682-088-693 PACKET in 1 BOX (47682-088-69) / 2 TABLET, CHEWABLE in 1 PACKET
647682-088-992 TABLET, CHEWABLE in 1 PACKET (47682-088-99)

NDC Record

Field Name Field Value Definition
PRODUCT NDC47682-088The 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 NAMEMedique AlcalakThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/30/2008This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH FINALProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERpart331This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEUnifirst First Aid CorporationName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 7/25/2025

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