Product NDC: | 15338-170 |
Proprietary Name: | Folic Acid |
Non Proprietary Name: | Folic Acid |
Active Ingredient(s): | 1 mg/1 & nbsp; Folic Acid |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 15338-170 |
Labeler Name: | Apace Packaging |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA080680 |
Marketing Category: | NDA |
Start Marketing Date: | 20091223 |
Package NDC: | 15338-170-00 |
Package Description: | 48 BOTTLE in 1 CARTON (15338-170-00) > 100 TABLET in 1 BOTTLE |
NDC Code | 15338-170-00 |
Proprietary Name | Folic Acid |
Package Description | 48 BOTTLE in 1 CARTON (15338-170-00) > 100 TABLET in 1 BOTTLE |
Product NDC | 15338-170 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Folic Acid |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20091223 |
Marketing Category Name | NDA |
Labeler Name | Apace Packaging |
Substance Name | FOLIC ACID |
Strength Number | 1 |
Strength Unit | mg/1 |
Pharmaceutical Classes |