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SORBITOL
SORBITOL - 57896-435-16 - (sorbitol)
Drug Information of SORBITOL
| Product NDC: | 57896-435 |
| Proprietary Name: | SORBITOL |
| Non Proprietary Name: | sorbitol |
| Active Ingredient(s): | 13.5 g/15mL & nbsp; sorbitol |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SORBITOL
| Product NDC: | 57896-435 |
| Labeler Name: | Geri-Care Pharmaceuticals, Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20000101 |
Package Information of SORBITOL
| Package NDC: | 57896-435-16 |
| Package Description: | 473 mL in 1 BOTTLE (57896-435-16) |
NDC Information of SORBITOL
| NDC Code | 57896-435-16 |
| Proprietary Name | SORBITOL |
| Package Description | 473 mL in 1 BOTTLE (57896-435-16) |
| Product NDC | 57896-435 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | sorbitol |
| Dosage Form Name | SOLUTION |
| Route Name | RECTAL |
| Start Marketing Date | 20000101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Geri-Care Pharmaceuticals, Corp |
| Substance Name | SORBITOL |
| Strength Number | 13.5 |
| Strength Unit | g/15mL |
| Pharmaceutical Classes |
