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Phenazopyridine HCl
Phenazopyridine HCl - 52959-122-30 - (Phenazopyridine HCl)
Drug Information of Phenazopyridine HCl
| Product NDC: | 52959-122 |
| Proprietary Name: | Phenazopyridine HCl |
| Non Proprietary Name: | Phenazopyridine HCl |
| Active Ingredient(s): | 200 mg/1 & nbsp; Phenazopyridine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phenazopyridine HCl
| Product NDC: | 52959-122 |
| Labeler Name: | H.J. Harkins Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100910 |
Package Information of Phenazopyridine HCl
| Package NDC: | 52959-122-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (52959-122-30) |
NDC Information of Phenazopyridine HCl
| NDC Code | 52959-122-30 |
| Proprietary Name | Phenazopyridine HCl |
| Package Description | 30 TABLET in 1 BOTTLE (52959-122-30) |
| Product NDC | 52959-122 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenazopyridine HCl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100910 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | PHENAZOPYRIDINE HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
