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Laxacin
Laxacin - 50488-0901-1 - (Docusate sodium and sennosides)
Drug Information of Laxacin
| Product NDC: | 50488-0901 |
| Proprietary Name: | Laxacin |
| 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 |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Laxacin
| Product NDC: | 50488-0901 |
| Labeler Name: | Alexso Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111001 |
Package Information of Laxacin
| Package NDC: | 50488-0901-1 |
| Package Description: | 100 TABLET in 1 BOTTLE (50488-0901-1) |
NDC Information of Laxacin
| NDC Code | 50488-0901-1 |
| Proprietary Name | Laxacin |
| Package Description | 100 TABLET in 1 BOTTLE (50488-0901-1) |
| Product NDC | 50488-0901 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Docusate sodium and sennosides |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111001 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Alexso Inc |
| Substance Name | DOCUSATE SODIUM; SENNOSIDES A AND B |
| Strength Number | 50; 8.6 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
