Ampicillin - 0781-2144-05 - (Ampicillin)

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Drug Information of Ampicillin

Product NDC: 0781-2144
Proprietary Name: Ampicillin
Non Proprietary Name: Ampicillin
Active Ingredient(s): 250    mg/1 & nbsp;   Ampicillin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Ampicillin

Product NDC: 0781-2144
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064082
Marketing Category: ANDA
Start Marketing Date: 19950829

Package Information of Ampicillin

Package NDC: 0781-2144-05
Package Description: 500 CAPSULE in 1 BOTTLE (0781-2144-05)

NDC Information of Ampicillin

NDC Code 0781-2144-05
Proprietary Name Ampicillin
Package Description 500 CAPSULE in 1 BOTTLE (0781-2144-05)
Product NDC 0781-2144
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ampicillin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19950829
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name AMPICILLIN TRIHYDRATE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Ampicillin


General Information