55603-671 NDC - ALUMINUM HYDROXIDE

Drug Information

  • Product NDC: 55603-671
  • Proprietary Name:
  • Non Proprietary Name: Aluminum Hydroxide
  • Active Ingredient(s): 1 kg/kg ALGELDRATE
  • Administration Route(s):
  • Dosage Form(s): PASTE

Labeler Information

Field Name Field Value
Labeler Name: Elementis Pharma Gmbh
Product Type: BULK INGREDIENT
FDA Application Number:
Marketing Category: BULK INGREDIENT
Start Marketing Date:9/22/2010

Package Information

No. Package Code Package Description Billing Unit
155603-671-51130 kg in 1 DRUM (55603-671-51)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55603-671The 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.
PRODUCT TYPE NAMEBULK INGREDIENTThe 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.
NON PROPRIETARY NAMEAluminum HydroxideThe 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.
DOSAGE FORM NAMEPASTEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/22/2010The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
MARKETING CATEGORY NAMEBULK INGREDIENTThe translation of the dosage form Code submitted by the firm.
LABELER NAMEElementis Pharma GmbhThe translation of the route code submitted by the firm, indicating route of administration.
SUBSTANCE NAMEALGELDRATEThis is the date that the labeler indicates was the start of its marketing of the drug product.
ACTIVE NUMERATOR STRENGTH1Product 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.
ACTIVE INGRED UNITkg/kg 

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This page was last updated on: 12/6/2025

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