Product NDC: | 0781-2145 |
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) |
Product NDC: | 0781-2145 |
Labeler Name: | Sandoz Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA064082 |
Marketing Category: | ANDA |
Start Marketing Date: | 19950829 |
Package NDC: | 0781-2145-01 |
Package Description: | 100 CAPSULE in 1 BOTTLE (0781-2145-01) |
NDC Code | 0781-2145-01 |
Proprietary Name | Ampicillin |
Package Description | 100 CAPSULE in 1 BOTTLE (0781-2145-01) |
Product NDC | 0781-2145 |
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 | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |