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Fludrocortisone Acetate
Fludrocortisone Acetate - 0555-0997-02 - (Fludrocortisone Acetate)
Drug Information of Fludrocortisone Acetate
| Product NDC: | 0555-0997 |
| Proprietary Name: | Fludrocortisone Acetate |
| Non Proprietary Name: | Fludrocortisone Acetate |
| Active Ingredient(s): | .1 mg/1 & nbsp; Fludrocortisone Acetate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fludrocortisone Acetate
| Product NDC: | 0555-0997 |
| Labeler Name: | Barr Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040425 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030214 |
Package Information of Fludrocortisone Acetate
| Package NDC: | 0555-0997-02 |
| Package Description: | 100 TABLET in 1 BOTTLE (0555-0997-02) |
NDC Information of Fludrocortisone Acetate
| NDC Code | 0555-0997-02 |
| Proprietary Name | Fludrocortisone Acetate |
| Package Description | 100 TABLET in 1 BOTTLE (0555-0997-02) |
| Product NDC | 0555-0997 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fludrocortisone Acetate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20030214 |
| Marketing Category Name | ANDA |
| Labeler Name | Barr Laboratories Inc. |
| Substance Name | FLUDROCORTISONE ACETATE |
| Strength Number | .1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
