50090-3150 NDC - ORPHENADRINE CITRATE ()

Drug Information

Product NDC: 50090-3150

Proprietary Name: Orphenadrine Citrate

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:6/23/2000

Package Information

No. Package Code Package Description Billing Unit
150090-3150-020 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-3150-0)EA
250090-3150-130 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-3150-1)EA
350090-3150-214 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-3150-2)
450090-3150-560 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-3150-5)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC50090-3150The 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 NAMEOrphenadrine CitrateThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/23/2000This 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