61919-088 NDC - DIAZEPAM ()

Drug Information

Product NDC: 61919-088

Proprietary Name: DIAZEPAM

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Direct_Rx
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/10/2019

Package Information

No. Package Code Package Description Billing Unit
161919-088-022 TABLET in 1 BOTTLE (61919-088-02)EA
261919-088-033 TABLET in 1 BOTTLE (61919-088-03)EA
361919-088-3030 TABLET in 1 BOTTLE (61919-088-30)EA
461919-088-6060 TABLET in 1 BOTTLE (61919-088-60)EA
561919-088-72120 TABLET in 1 BOTTLE (61919-088-72)EA
661919-088-9090 TABLET in 1 BOTTLE (61919-088-90)

NDC Record

Field Name Field Value Definition
PRODUCT NDC61919-088The 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 NAMEDIAZEPAMThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/7/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDIRECT RXName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC61919-088The 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 NAMEDIAZEPAMThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/10/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDirect_RxName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC61919-088The 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 NAMEDIAZEPAMThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/10/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDirect_RxName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023