Product NDC: | 67253-183 |
Proprietary Name: | Ampicillin |
Non Proprietary Name: | Ampicillin Trihydrate |
Active Ingredient(s): | 50 mg/mL & nbsp; Ampicillin Trihydrate |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67253-183 |
Labeler Name: | DAVA Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA062982 |
Marketing Category: | ANDA |
Start Marketing Date: | 19890210 |
Package NDC: | 67253-183-20 |
Package Description: | 200 mL in 1 BOTTLE, PLASTIC (67253-183-20) |
NDC Code | 67253-183-20 |
Proprietary Name | Ampicillin |
Package Description | 200 mL in 1 BOTTLE, PLASTIC (67253-183-20) |
Product NDC | 67253-183 |
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 | 50 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |