Ampicillin - 55289-023-20 - (Ampicillin)

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Drug Information of Ampicillin

Product NDC: 55289-023
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: 55289-023
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064082
Marketing Category: ANDA
Start Marketing Date: 19950829

Package Information of Ampicillin

Package NDC: 55289-023-20
Package Description: 20 CAPSULE in 1 BOTTLE, PLASTIC (55289-023-20)

NDC Information of Ampicillin

NDC Code 55289-023-20
Proprietary Name Ampicillin
Package Description 20 CAPSULE in 1 BOTTLE, PLASTIC (55289-023-20)
Product NDC 55289-023
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 PD-Rx Pharmaceuticals, 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


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