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LACTULOSE
LACTULOSE - 66689-038-50 - (LACTULOSE)
Drug Information of LACTULOSE
| Product NDC: | 66689-038 |
| Proprietary Name: | LACTULOSE |
| Non Proprietary Name: | LACTULOSE |
| Active Ingredient(s): | 20 g/30mL & nbsp; LACTULOSE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LACTULOSE
| Product NDC: | 66689-038 |
| Labeler Name: | VistaPharm, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074138 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100510 |
Package Information of LACTULOSE
| Package NDC: | 66689-038-50 |
| Package Description: | 5 TRAY in 1 CASE (66689-038-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 30 mL in 1 CUP, UNIT-DOSE (66689-038-01) |
NDC Information of LACTULOSE
| NDC Code | 66689-038-50 |
| Proprietary Name | LACTULOSE |
| Package Description | 5 TRAY in 1 CASE (66689-038-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 30 mL in 1 CUP, UNIT-DOSE (66689-038-01) |
| Product NDC | 66689-038 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LACTULOSE |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20100510 |
| Marketing Category Name | ANDA |
| Labeler Name | VistaPharm, Inc |
| Substance Name | LACTULOSE |
| Strength Number | 20 |
| Strength Unit | g/30mL |
| Pharmaceutical Classes | Osmotic Laxative [EPC],Osmotic Activity [MoA],Acidifying Activity [MoA],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |
