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P LAX DR
P LAX DR - 68210-0002-7 - (BISACODYL)
Drug Information of P LAX DR
| Product NDC: | 68210-0002 |
| Proprietary Name: | P LAX DR |
| Non Proprietary Name: | BISACODYL |
| Active Ingredient(s): | 5 mg/1 & nbsp; BISACODYL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, SUGAR COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of P LAX DR
| Product NDC: | 68210-0002 |
| Labeler Name: | SPIRIT PHARMACEUTICALS,LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100501 |
Package Information of P LAX DR
| Package NDC: | 68210-0002-7 |
| Package Description: | 1 BAG in 1 DRUM (68210-0002-7) > 70000 TABLET, SUGAR COATED in 1 BAG |
NDC Information of P LAX DR
| NDC Code | 68210-0002-7 |
| Proprietary Name | P LAX DR |
| Package Description | 1 BAG in 1 DRUM (68210-0002-7) > 70000 TABLET, SUGAR COATED in 1 BAG |
| Product NDC | 68210-0002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BISACODYL |
| Dosage Form Name | TABLET, SUGAR COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100501 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SPIRIT PHARMACEUTICALS,LLC |
| Substance Name | BISACODYL |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
