| Product NDC: | 21695-124 |
| 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: | 21695-124 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA061454 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19710401 |
| Package NDC: | 21695-124-30 |
| Package Description: | 30 CAPSULE in 1 BOTTLE (21695-124-30) |
| NDC Code | 21695-124-30 |
| Proprietary Name | Dicloxacillin Sodium |
| Package Description | 30 CAPSULE in 1 BOTTLE (21695-124-30) |
| Product NDC | 21695-124 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dicloxacillin Sodium |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19710401 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | DICLOXACILLIN SODIUM |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |