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Phentermine Hydrochloride - 0093-2110-01 - (Phentermine Hydrochloride)

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Drug Information of Phentermine Hydrochloride

Product NDC: 0093-2110
Proprietary Name: Phentermine Hydrochloride
Non Proprietary Name: Phentermine Hydrochloride
Active Ingredient(s): 15    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: 0093-2110
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090591
Marketing Category: ANDA
Start Marketing Date: 20110309

Package Information of Phentermine Hydrochloride

Package NDC: 0093-2110-01
Package Description: 100 CAPSULE in 1 BOTTLE (0093-2110-01)

NDC Information of Phentermine Hydrochloride

NDC Code 0093-2110-01
Proprietary Name Phentermine Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (0093-2110-01)
Product NDC 0093-2110
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phentermine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110309
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name PHENTERMINE HYDROCHLORIDE
Strength Number 15
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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