25021-159 NDC - COLISTIMETHATE ()

Drug Information

  • Product NDC: 25021-159
  • Proprietary Name: Colistimethate
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Sagent Pharmaceuticals
Product Type:
FDA Application Number: ANDA201365
Marketing Category: ANDA
Start Marketing Date:12/29/2014
End Marketing Date:9/30/2019

Package Information

No. Package Code Package Description Billing Unit
125021-159-101 VIAL in 1 CARTON (25021-159-10) / 2 mL in 1 VIALEA

NDC Record

Field Name Field Value Definition
PRODUCT NDC25021-159The 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 NAMEColistimethateThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/29/2014The 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.
END MARKETING DATE9/30/2019Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
MARKETING CATEGORY NAMEANDAThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
APPLICATION NUMBERANDA201365This 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 NAMESagent PharmaceuticalsName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 11/21/2025

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