67877-210 NDC - ZALEPLON ()

Drug Information

Product NDC: 67877-210

Proprietary Name: ZALEPLON

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Ascend Laboratories, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/15/2010

Package Information

No. Package Code Package Description Billing Unit
167877-210-01100 CAPSULE in 1 BOTTLE (67877-210-01)EA
267877-210-05500 CAPSULE in 1 BOTTLE (67877-210-05)
367877-210-3030 CAPSULE in 1 BOTTLE (67877-210-30)

NDC Record

Field Name Field Value Definition
PRODUCT NDC67877-210The 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 NAMEZALEPLONThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/15/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAscend Laboratories, LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 11/18/2019