Ampicillin - 67253-182-20 - (Ampicillin Trihydrate)

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Drug Information of Ampicillin

Product NDC: 67253-182
Proprietary Name: Ampicillin
Non Proprietary Name: Ampicillin Trihydrate
Active Ingredient(s): 25    mg/mL & nbsp;   Ampicillin Trihydrate
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Ampicillin

Product NDC: 67253-182
Labeler Name: DAVA Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062982
Marketing Category: ANDA
Start Marketing Date: 19890210

Package Information of Ampicillin

Package NDC: 67253-182-20
Package Description: 200 mL in 1 BOTTLE, PLASTIC (67253-182-20)

NDC Information of Ampicillin

NDC Code 67253-182-20
Proprietary Name Ampicillin
Package Description 200 mL in 1 BOTTLE, PLASTIC (67253-182-20)
Product NDC 67253-182
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ampicillin Trihydrate
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 19890210
Marketing Category Name ANDA
Labeler Name DAVA Pharmaceuticals, Inc.
Substance Name AMPICILLIN TRIHYDRATE
Strength Number 25
Strength Unit mg/mL
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Ampicillin


General Information