Product NDC: | 0904-5666 |
Proprietary Name: | phosphate |
Non Proprietary Name: | dibasic sodium phosphate, monobasic sodium phosphate |
Active Ingredient(s): | 2.9; 7.2 g/15mL; g/15mL & nbsp; dibasic sodium phosphate, monobasic sodium phosphate |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0904-5666 |
Labeler Name: | Major Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100602 |
Package NDC: | 0904-5666-75 |
Package Description: | 1 BOTTLE in 1 CARTON (0904-5666-75) > 45 mL in 1 BOTTLE |
NDC Code | 0904-5666-75 |
Proprietary Name | phosphate |
Package Description | 1 BOTTLE in 1 CARTON (0904-5666-75) > 45 mL in 1 BOTTLE |
Product NDC | 0904-5666 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | dibasic sodium phosphate, monobasic sodium phosphate |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20100602 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Major Pharmaceuticals |
Substance Name | SODIUM PHOSPHATE, DIBASIC; SODIUM PHOSPHATE, MONOBASIC |
Strength Number | 2.9; 7.2 |
Strength Unit | g/15mL; g/15mL |
Pharmaceutical Classes |