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Leucovorin Calcium
Leucovorin Calcium - 0555-0485-27 - (Leucovorin Calcium)
Drug Information of Leucovorin Calcium
| Product NDC: | 0555-0485 |
| 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) |
Labeler Information of Leucovorin Calcium
| Product NDC: | 0555-0485 |
| Labeler Name: | Barr Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071199 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19900630 |
Package Information of Leucovorin Calcium
| Package NDC: | 0555-0485-27 |
| Package Description: | 25 TABLET in 1 BOTTLE (0555-0485-27) |
NDC Information of Leucovorin Calcium
| NDC Code | 0555-0485-27 |
| Proprietary Name | Leucovorin Calcium |
| Package Description | 25 TABLET in 1 BOTTLE (0555-0485-27) |
| Product NDC | 0555-0485 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Leucovorin Calcium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19900630 |
| Marketing Category Name | ANDA |
| Labeler Name | Barr Laboratories Inc. |
| Substance Name | LEUCOVORIN CALCIUM |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Folate Analog [EPC],Folic Acid [Chemical/Ingredient] |
