Product NDC: | 0054-4499 |
Proprietary Name: | Leucovorin Calcium |
Non Proprietary Name: | Leucovorin Calcium |
Active Ingredient(s): | 25 mg/1 & nbsp; Leucovorin Calcium |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0054-4499 |
Labeler Name: | Roxane Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA072736 |
Marketing Category: | ANDA |
Start Marketing Date: | 19930222 |
Package NDC: | 0054-4499-11 |
Package Description: | 25 TABLET in 1 BOTTLE (0054-4499-11) |
NDC Code | 0054-4499-11 |
Proprietary Name | Leucovorin Calcium |
Package Description | 25 TABLET in 1 BOTTLE (0054-4499-11) |
Product NDC | 0054-4499 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Leucovorin Calcium |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19930222 |
Marketing Category Name | ANDA |
Labeler Name | Roxane Laboratories, Inc. |
Substance Name | LEUCOVORIN CALCIUM |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Folate Analog [EPC],Folic Acid [Chemical/Ingredient] |