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: | 76439-206-30 |
Package Description: | 30 TABLET, COATED in 1 BOTTLE (76439-206-30) |
NDC Code | 76439-206-30 |
Proprietary Name | L-Methylfolate Calcium |
Package Description | 30 TABLET, COATED in 1 BOTTLE (76439-206-30) |
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 |