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L-Methylfolate Calcium - 76439-206-30 - (LEVOMEFOLATE CALCIUM)

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Drug Information of L-Methylfolate Calcium

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)

Labeler Information of L-Methylfolate Calcium

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 Information of L-Methylfolate Calcium

Package NDC: 76439-206-30
Package Description: 30 TABLET, COATED in 1 BOTTLE (76439-206-30)

NDC Information of L-Methylfolate Calcium

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

Complete Information of L-Methylfolate Calcium


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