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Sunmark Urinary Pain Relief Maximum Strength
Sunmark Urinary Pain Relief Maximum Strength - 49348-941-01 - (PHENAZOPYRIDINE HYDROCHLORIDE)
Drug Information of Sunmark Urinary Pain Relief Maximum Strength
| Product NDC: | 49348-941 |
| Proprietary Name: | Sunmark Urinary Pain Relief Maximum Strength |
| 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 Sunmark Urinary Pain Relief Maximum Strength
| Product NDC: | 49348-941 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110910 |
Package Information of Sunmark Urinary Pain Relief Maximum Strength
| Package NDC: | 49348-941-01 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (49348-941-01) > 12 TABLET in 1 BLISTER PACK (49348-941-02) |
NDC Information of Sunmark Urinary Pain Relief Maximum Strength
| NDC Code | 49348-941-01 |
| Proprietary Name | Sunmark Urinary Pain Relief Maximum Strength |
| Package Description | 1 BLISTER PACK in 1 CARTON (49348-941-01) > 12 TABLET in 1 BLISTER PACK (49348-941-02) |
| Product NDC | 49348-941 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | PHENAZOPYRIDINE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110910 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | McKesson |
| Substance Name | PHENAZOPYRIDINE HYDROCHLORIDE |
| Strength Number | 97.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
