Product NDC: | 54868-0937 |
Proprietary Name: | Dicloxacillin Sodium |
Non Proprietary Name: | Dicloxacillin Sodium |
Active Ingredient(s): | 250 mg/1 & nbsp; Dicloxacillin Sodium |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-0937 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA061454 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040817 |
Package NDC: | 54868-0937-2 |
Package Description: | 40 CAPSULE in 1 BOTTLE, PLASTIC (54868-0937-2) |
NDC Code | 54868-0937-2 |
Proprietary Name | Dicloxacillin Sodium |
Package Description | 40 CAPSULE in 1 BOTTLE, PLASTIC (54868-0937-2) |
Product NDC | 54868-0937 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Dicloxacillin Sodium |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20040817 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | DICLOXACILLIN SODIUM |
Strength Number | 250 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |