Ampicillin - 0069-0029-18 - (Ampicillin Sodium)

Alphabetical Index


Drug Information of Ampicillin

Product NDC: 0069-0029
Proprietary Name: Ampicillin
Non Proprietary Name: Ampicillin Sodium
Active Ingredient(s): 1    g/1 & nbsp;   Ampicillin Sodium
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ampicillin

Product NDC: 0069-0029
Labeler Name: Pfizer Laboratories, Division of Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065499
Marketing Category: ANDA
Start Marketing Date: 20100817

Package Information of Ampicillin

Package NDC: 0069-0029-18
Package Description: 10 VIAL in 1 BOX (0069-0029-18) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0069-0029-20)

NDC Information of Ampicillin

NDC Code 0069-0029-18
Proprietary Name Ampicillin
Package Description 10 VIAL in 1 BOX (0069-0029-18) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0069-0029-20)
Product NDC 0069-0029
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ampicillin Sodium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20100817
Marketing Category Name ANDA
Labeler Name Pfizer Laboratories, Division of Pfizer Inc
Substance Name AMPICILLIN SODIUM
Strength Number 1
Strength Unit g/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Ampicillin


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