33261-408 NDC - PHENTERMINE HYDROCHLORIDE ()

Drug Information

Product NDC: 33261-408

Proprietary Name: Phentermine Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Aidarex Pharmaceuticals LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/15/2012

Package Information

No. Package Code Package Description Billing Unit
133261-408-077 CAPSULE in 1 BOTTLE (33261-408-07)EA
233261-408-088 CAPSULE in 1 BOTTLE (33261-408-08)
333261-408-1414 CAPSULE in 1 BOTTLE (33261-408-14)EA
433261-408-1515 CAPSULE in 1 BOTTLE (33261-408-15)
533261-408-2323 CAPSULE in 1 BOTTLE (33261-408-23)
633261-408-2828 CAPSULE in 1 BOTTLE (33261-408-28)EA
733261-408-3030 CAPSULE in 1 BOTTLE (33261-408-30)EA
833261-408-4040 CAPSULE in 1 BOTTLE (33261-408-40)
933261-408-4545 CAPSULE in 1 BOTTLE (33261-408-45)
1033261-408-6060 CAPSULE in 1 BOTTLE (33261-408-60)

NDC Record

Field Name Field Value Definition
PRODUCT NDC33261-408The 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 NAMEPhentermine 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 DATE8/15/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAidarex Pharmaceuticals LLCName 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