| Product NDC: | 76439-206 |
| Proprietary Name: | L-Methylfolate Calcium |
| Non Proprietary Name: | LEVOMEFOLATE CALCIUM |
| Active Ingredient(s): | 7.5 mg/1 & nbsp; LEVOMEFOLATE CALCIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76439-206 |
| Labeler Name: | Virtus Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120315 |
| Package NDC: | 76439-206-90 |
| Package Description: | 90 TABLET, COATED in 1 BOTTLE (76439-206-90) |
| NDC Code | 76439-206-90 |
| Proprietary Name | L-Methylfolate Calcium |
| Package Description | 90 TABLET, COATED in 1 BOTTLE (76439-206-90) |
| Product NDC | 76439-206 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LEVOMEFOLATE CALCIUM |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120315 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Virtus Pharmaceuticals |
| Substance Name | LEVOMEFOLATE CALCIUM |
| Strength Number | 7.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |