Product NDC: | 21695-307 |
Proprietary Name: | Prednisone |
Non Proprietary Name: | Prednisone |
Active Ingredient(s): | 20 mg/1 & nbsp; Prednisone |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-307 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA083677 |
Marketing Category: | ANDA |
Start Marketing Date: | 19740226 |
Package NDC: | 21695-307-21 |
Package Description: | 21 TABLET in 1 BOTTLE (21695-307-21) |
NDC Code | 21695-307-21 |
Proprietary Name | Prednisone |
Package Description | 21 TABLET in 1 BOTTLE (21695-307-21) |
Product NDC | 21695-307 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Prednisone |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19740226 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | PREDNISONE |
Strength Number | 20 |
Strength Unit | mg/1 |
Pharmaceutical Classes |