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Urinary Pain Relief
Urinary Pain Relief - 49348-364-44 - (Phenazopyridine Hydrochloride)
Drug Information of Urinary Pain Relief
| Product NDC: | 49348-364 |
| Proprietary Name: | Urinary Pain Relief |
| Non Proprietary Name: | Phenazopyridine Hydrochloride |
| Active Ingredient(s): | 95 mg/1 & nbsp; Phenazopyridine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Urinary Pain Relief
| Product NDC: | 49348-364 |
| Labeler Name: | Mckesson (Sunmark) |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100709 |
Package Information of Urinary Pain Relief
| Package NDC: | 49348-364-44 |
| Package Description: | 1 CELLO PACK in 1 CARTON (49348-364-44) > 30 TABLET in 1 CELLO PACK |
NDC Information of Urinary Pain Relief
| NDC Code | 49348-364-44 |
| Proprietary Name | Urinary Pain Relief |
| Package Description | 1 CELLO PACK in 1 CARTON (49348-364-44) > 30 TABLET in 1 CELLO PACK |
| Product NDC | 49348-364 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Phenazopyridine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100709 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Mckesson (Sunmark) |
| Substance Name | PHENAZOPYRIDINE HYDROCHLORIDE |
| Strength Number | 95 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
