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womens laxative
womens laxative - 50804-120-30 - (Bisacodyl)
Drug Information of womens laxative
| Product NDC: | 50804-120 |
| Proprietary Name: | womens laxative |
| Non Proprietary Name: | Bisacodyl |
| Active Ingredient(s): | 5 mg/1 & nbsp; Bisacodyl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of womens laxative
| Product NDC: | 50804-120 |
| Labeler Name: | Good Sense (Geiss, Destin & Dunn, Inc.) |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130416 |
Package Information of womens laxative
| Package NDC: | 50804-120-30 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (50804-120-30) > 15 TABLET in 1 BLISTER PACK |
NDC Information of womens laxative
| NDC Code | 50804-120-30 |
| Proprietary Name | womens laxative |
| Package Description | 2 BLISTER PACK in 1 CARTON (50804-120-30) > 15 TABLET in 1 BLISTER PACK |
| Product NDC | 50804-120 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bisacodyl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130416 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Good Sense (Geiss, Destin & Dunn, Inc.) |
| Substance Name | BISACODYL |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
