55648-140 NDC - LANSOPRAZOLE ()

Drug Information

Product NDC: 55648-140

Proprietary Name: Lansoprazole

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Wockhardt Limited
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/18/2012

Package Information

No. Package Code Package Description Billing Unit
155648-140-004500 CAPSULE, DELAYED RELEASE in 1 POUCH (55648-140-00)
255648-140-011 BOTTLE in 1 CARTON (55648-140-01) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
355648-140-071 BLISTER PACK in 1 CARTON (55648-140-07) / 14 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
455648-140-082 BOTTLE in 1 CARTON (55648-140-08) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
555648-140-093 BOTTLE in 1 CARTON (55648-140-09) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
655648-140-102 BLISTER PACK in 1 CARTON (55648-140-10) / 14 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
755648-140-113 BLISTER PACK in 1 CARTON (55648-140-11) / 14 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

NDC Record

Field Name Field Value Definition
PRODUCT NDC55648-140The 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 NAMELansoprazoleThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/18/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEWockhardt LimitedName 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