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SENEXON-S
SENEXON-S - 52959-675-30 - (DOCUSATE SODIUM -SENNOSIDES)
Drug Information of SENEXON-S
| Product NDC: | 52959-675 |
| Proprietary Name: | SENEXON-S |
| Non Proprietary Name: | DOCUSATE SODIUM -SENNOSIDES |
| Active Ingredient(s): | 50; 8.6 mg/1; mg/1 & nbsp; DOCUSATE SODIUM -SENNOSIDES |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SENEXON-S
| Product NDC: | 52959-675 |
| Labeler Name: | H.J. Harkins Company, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110316 |
Package Information of SENEXON-S
| Package NDC: | 52959-675-30 |
| Package Description: | 30 TABLET, COATED in 1 BOTTLE, PLASTIC (52959-675-30) |
NDC Information of SENEXON-S
| NDC Code | 52959-675-30 |
| Proprietary Name | SENEXON-S |
| Package Description | 30 TABLET, COATED in 1 BOTTLE, PLASTIC (52959-675-30) |
| Product NDC | 52959-675 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DOCUSATE SODIUM -SENNOSIDES |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110316 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | DOCUSATE SODIUM; SENNOSIDES A AND B |
| Strength Number | 50; 8.6 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
