61919-133 NDC - HALOPERIDOL ()

Drug Information

  • Product NDC: 61919-133
  • Proprietary Name: HALOPERIDOL
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: DIRECT RX
Product Type:
FDA Application Number: ANDA077580
Marketing Category: ANDA
Start Marketing Date:1/1/2014

Package Information

No. Package Code Package Description Billing Unit
161919-133-3030 TABLET in 1 BOTTLE (61919-133-30)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC61919-133The 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 NAMEHALOPERIDOLThis is the date that the labeler indicates was the start of its marketing of the drug product.
START MARKETING DATE1/1/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEANDAThe 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.
APPLICATION NUMBERANDA077580This 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 NAMEDIRECT RXThis 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.

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

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