69097-315 NDC - LAMIVUDINE AND ZIDOVUDINE ()

Drug Information

Product NDC: 69097-315

Proprietary Name: Lamivudine and Zidovudine

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	69097-315-02	30 TABLET, FILM COATED in 1 BOTTLE (69097-315-02)
2	69097-315-03	60 TABLET, FILM COATED in 1 BOTTLE (69097-315-03)
3	69097-315-15	1000 TABLET, FILM COATED in 1 BOTTLE (69097-315-15)
4	69097-315-21	10 BLISTER PACK in 1 BOX, UNIT-DOSE (69097-315-21) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Field Name	Field Value	Definition
PRODUCT NDC	69097-315	The 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 NAME	Lamivudine and Zidovudine	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	9/7/2018	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Cipla USA Inc.	Name 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