57297-333 NDC - ZIPRASIDONE HYDROCHLORIDE ()

Drug Information

  • Product NDC: 57297-333
  • Proprietary Name: Ziprasidone Hydrochloride
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: LUPIN LIMITED
Product Type:
FDA Application Number: ANDA077560
Marketing Category: ANDA
Start Marketing Date:3/2/2012
End Marketing Date:9/30/2021

Package Information

No. Package Code Package Description Billing Unit
157297-333-0760 CAPSULE in 1 BOTTLE (57297-333-07)

NDC Record

Field Name Field Value Definition
PRODUCT NDC57297-333This 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.
PROPRIETARY NAMEZiprasidone HydrochlorideAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
START MARKETING DATE3/2/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE9/30/2021This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
MARKETING CATEGORY NAMEANDA 
APPLICATION NUMBERANDA077560 
LABELER NAMELUPIN LIMITED 

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This page was last updated on: 1/2/2026

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