Ampicillin - 52959-389-20 - (Ampicillin)

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Drug Information of Ampicillin

Product NDC: 52959-389
Proprietary Name: Ampicillin
Non Proprietary Name: Ampicillin
Active Ingredient(s): 500    mg/1 & nbsp;   Ampicillin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Ampicillin

Product NDC: 52959-389
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062882
Marketing Category: ANDA
Start Marketing Date: 19880225

Package Information of Ampicillin

Package NDC: 52959-389-20
Package Description: 20 CAPSULE in 1 BOTTLE, PLASTIC (52959-389-20)

NDC Information of Ampicillin

NDC Code 52959-389-20
Proprietary Name Ampicillin
Package Description 20 CAPSULE in 1 BOTTLE, PLASTIC (52959-389-20)
Product NDC 52959-389
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ampicillin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19880225
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name AMPICILLIN TRIHYDRATE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Ampicillin


General Information