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Dulcolax
Dulcolax - 0597-0016-18 - (docusate sodium)
Drug Information of Dulcolax
| Product NDC: | 0597-0016 |
| Proprietary Name: | Dulcolax |
| Non Proprietary Name: | docusate sodium |
| Active Ingredient(s): | 100 mg/1 & nbsp; docusate sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dulcolax
| Product NDC: | 0597-0016 |
| Labeler Name: | Boehringer Ingelheim Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20021001 |
Package Information of Dulcolax
| Package NDC: | 0597-0016-18 |
| Package Description: | 180 GEL in 1 BOTTLE (0597-0016-18) |
NDC Information of Dulcolax
| NDC Code | 0597-0016-18 |
| Proprietary Name | Dulcolax |
| Package Description | 180 GEL in 1 BOTTLE (0597-0016-18) |
| Product NDC | 0597-0016 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | docusate sodium |
| Dosage Form Name | GEL |
| Route Name | ORAL |
| Start Marketing Date | 20021001 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Boehringer Ingelheim Pharmaceuticals, Inc. |
| Substance Name | DOCUSATE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
