50090-3250 NDC - ACYCLOVIR ()

Drug Information

Product NDC: 50090-3250

Proprietary Name: acyclovir

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: A-S Medication Solutions
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/10/2014

Package Information

No. Package Code Package Description Billing Unit
150090-3250-225 TABLET in 1 BOTTLE (50090-3250-2)EA
250090-3250-350 TABLET in 1 BOTTLE (50090-3250-3)EA
350090-3250-415 TABLET in 1 BOTTLE (50090-3250-4)EA
450090-3250-530 TABLET in 1 BOTTLE (50090-3250-5)EA
550090-3250-660 TABLET in 1 BOTTLE (50090-3250-6)EA
650090-3250-945 TABLET in 1 BOTTLE (50090-3250-9)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC50090-3250The 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 NAMEacyclovirThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/10/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEA-S Medication SolutionsName 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