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LEADER MAXIMUM STRENGHT URINARY PAIN RELIEF
LEADER MAXIMUM STRENGHT URINARY PAIN RELIEF - 37205-630-01 - (PHENAZOPYRIDINE HYDROCHLORIDE)
Drug Information of LEADER MAXIMUM STRENGHT URINARY PAIN RELIEF
| Product NDC: | 37205-630 |
| Proprietary Name: | LEADER MAXIMUM STRENGHT URINARY PAIN RELIEF |
| Non Proprietary Name: | PHENAZOPYRIDINE HYDROCHLORIDE |
| Active Ingredient(s): | 97.5 mg/1 & nbsp; PHENAZOPYRIDINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LEADER MAXIMUM STRENGHT URINARY PAIN RELIEF
| Product NDC: | 37205-630 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20090430 |
Package Information of LEADER MAXIMUM STRENGHT URINARY PAIN RELIEF
| Package NDC: | 37205-630-01 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (37205-630-01) > 12 TABLET in 1 BLISTER PACK (37205-630-53) |
NDC Information of LEADER MAXIMUM STRENGHT URINARY PAIN RELIEF
| NDC Code | 37205-630-01 |
| Proprietary Name | LEADER MAXIMUM STRENGHT URINARY PAIN RELIEF |
| Package Description | 1 BLISTER PACK in 1 CARTON (37205-630-01) > 12 TABLET in 1 BLISTER PACK (37205-630-53) |
| Product NDC | 37205-630 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | PHENAZOPYRIDINE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090430 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Cardinal Health |
| Substance Name | PHENAZOPYRIDINE HYDROCHLORIDE |
| Strength Number | 97.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
