| Product NDC: | 0132-0751 |
| Proprietary Name: | Fleet |
| Non Proprietary Name: | Docusate Sodium |
| Active Ingredient(s): | 100 mg/601 & nbsp; Docusate Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, GELATIN COATED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0132-0751 |
| Labeler Name: | C.B. Fleet Company, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20020630 |
| Package NDC: | 0132-0751-60 |
| Package Description: | 60 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (0132-0751-60) |
| NDC Code | 0132-0751-60 |
| Proprietary Name | Fleet |
| Package Description | 60 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (0132-0751-60) |
| Product NDC | 0132-0751 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Docusate Sodium |
| Dosage Form Name | CAPSULE, GELATIN COATED |
| Route Name | ORAL |
| Start Marketing Date | 20020630 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | C.B. Fleet Company, Inc. |
| Substance Name | DOCUSATE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/601 |
| Pharmaceutical Classes |