57844-187 NDC - ORAP ()

Drug Information

  • Product NDC: 57844-187
  • Proprietary Name: ORAP
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Teva Select Brands
Product Type:
FDA Application Number: NDA017473
Marketing Category: NDA
Start Marketing Date:9/30/1990
End Marketing Date:10/31/2017

Package Information

No. Package Code Package Description Billing Unit
157844-187-01100 TABLET in 1 BOTTLE (57844-187-01)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC57844-187The 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 NAMEORAPThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/30/1990This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE10/31/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMENDAIndicates 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.
APPLICATION NUMBERNDA017473The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
LABELER NAMETeva Select BrandsThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

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