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Phentermine Hydrochloride - 10702-029-01 - (Phentermine Hydrochloride)

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Drug Information of Phentermine Hydrochloride

Product NDC: 10702-029
Proprietary Name: Phentermine Hydrochloride
Non Proprietary Name: Phentermine Hydrochloride
Active Ingredient(s): 37.5    mg/1 & nbsp;   Phentermine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Phentermine Hydrochloride

Product NDC: 10702-029
Labeler Name: KVK-TECH, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040887
Marketing Category: ANDA
Start Marketing Date: 20120815

Package Information of Phentermine Hydrochloride

Package NDC: 10702-029-01
Package Description: 100 CAPSULE in 1 BOTTLE (10702-029-01)

NDC Information of Phentermine Hydrochloride

NDC Code 10702-029-01
Proprietary Name Phentermine Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (10702-029-01)
Product NDC 10702-029
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phentermine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120815
Marketing Category Name ANDA
Labeler Name KVK-TECH, Inc.
Substance Name PHENTERMINE HYDROCHLORIDE
Strength Number 37.5
Strength Unit mg/1
Pharmaceutical Classes Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]

Complete Information of Phentermine Hydrochloride


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