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Sunmark womans laxative
Sunmark womans laxative - 49348-223-44 - (Bisacodyl)
Drug Information of Sunmark womans laxative
| Product NDC: | 49348-223 |
| Proprietary Name: | Sunmark womans laxative |
| Non Proprietary Name: | Bisacodyl |
| Active Ingredient(s): | 5 mg/1 & nbsp; Bisacodyl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunmark womans laxative
| Product NDC: | 49348-223 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20030914 |
Package Information of Sunmark womans laxative
| Package NDC: | 49348-223-44 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (49348-223-44) > 15 TABLET, COATED in 1 BLISTER PACK |
NDC Information of Sunmark womans laxative
| NDC Code | 49348-223-44 |
| Proprietary Name | Sunmark womans laxative |
| Package Description | 2 BLISTER PACK in 1 CARTON (49348-223-44) > 15 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 49348-223 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bisacodyl |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20030914 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | McKesson |
| Substance Name | BISACODYL |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
