Product NDC: | 0904-0049 |
Proprietary Name: | formula em |
Non Proprietary Name: | Dextrose (glucose), Levulose (fructose), Phosphoric Acid |
Active Ingredient(s): | 1.87; 1.87; 21.5 g/5mL; g/5mL; mg/5mL & nbsp; Dextrose (glucose), Levulose (fructose), Phosphoric Acid |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0904-0049 |
Labeler Name: | Major Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19940415 |
Package NDC: | 0904-0049-20 |
Package Description: | 1 BOTTLE in 1 CARTON (0904-0049-20) > 118 mL in 1 BOTTLE |
NDC Code | 0904-0049-20 |
Proprietary Name | formula em |
Package Description | 1 BOTTLE in 1 CARTON (0904-0049-20) > 118 mL in 1 BOTTLE |
Product NDC | 0904-0049 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Dextrose (glucose), Levulose (fructose), Phosphoric Acid |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 19940415 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Major Pharmaceuticals |
Substance Name | DEXTROSE; FRUCTOSE; PHOSPHORIC ACID |
Strength Number | 1.87; 1.87; 21.5 |
Strength Unit | g/5mL; g/5mL; mg/5mL |
Pharmaceutical Classes |