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Senna-S
Senna-S - 0182-1113-10 - (Docusate sodium and Sennosides)
Drug Information of Senna-S
| Product NDC: | 0182-1113 |
| Proprietary Name: | Senna-S |
| Non Proprietary Name: | Docusate sodium and Sennosides |
| Active Ingredient(s): | 50; 8.6 mg/1; mg/1 & nbsp; Docusate sodium and Sennosides |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Senna-S
| Product NDC: | 0182-1113 |
| Labeler Name: | Goldline Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19990323 |
Package Information of Senna-S
| Package NDC: | 0182-1113-10 |
| Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0182-1113-10) |
NDC Information of Senna-S
| NDC Code | 0182-1113-10 |
| Proprietary Name | Senna-S |
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0182-1113-10) |
| Product NDC | 0182-1113 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Docusate sodium and Sennosides |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19990323 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Goldline Laboratories, Inc. |
| Substance Name | DOCUSATE SODIUM; SENNOSIDES |
| Strength Number | 50; 8.6 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
