55648-718 NDC - VENLAFAXINE HYDROCHLORIDE ()

Drug Information

Product NDC: 55648-718

Proprietary Name: VENLAFAXINE HYDROCHLORIDE

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:4/14/2011

Package Information

No. Package Code Package Description Billing Unit
155648-718-0130 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55648-718-01)
255648-718-021000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55648-718-02)
355648-718-0316 BLISTER PACK in 1 CARTON (55648-718-03) / 8 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
455648-718-0490 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55648-718-04)
555648-718-05500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55648-718-05)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55648-718The 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 NAMEVENLAFAXINE HYDROCHLORIDEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/14/2011This 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