Home
>
National Drug Code (NDC)
>
Sorbitol
Sorbitol - 52471-111-16 - (Sorbitol)
Drug Information of Sorbitol
| Product NDC: | 52471-111 |
| Proprietary Name: | Sorbitol |
| Non Proprietary Name: | Sorbitol |
| Active Ingredient(s): | 1 g/mL & nbsp; Sorbitol |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sorbitol
| Product NDC: | 52471-111 |
| Labeler Name: | H&H Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130610 |
Package Information of Sorbitol
| Package NDC: | 52471-111-16 |
| Package Description: | 473 mL in 1 BOTTLE (52471-111-16) |
NDC Information of Sorbitol
| NDC Code | 52471-111-16 |
| Proprietary Name | Sorbitol |
| Package Description | 473 mL in 1 BOTTLE (52471-111-16) |
| Product NDC | 52471-111 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sorbitol |
| Dosage Form Name | SOLUTION |
| Route Name | RECTAL |
| Start Marketing Date | 20130610 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | H&H Laboratories, Inc. |
| Substance Name | SORBITOL |
| Strength Number | 1 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |
