Product NDC: | 54569-0197 |
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) |
Product NDC: | 54569-0197 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100910 |
Package NDC: | 54569-0197-6 |
Package Description: | 12 TABLET in 1 BOTTLE (54569-0197-6) |
NDC Code | 54569-0197-6 |
Proprietary Name | Phenazopyridine HCl |
Package Description | 12 TABLET in 1 BOTTLE (54569-0197-6) |
Product NDC | 54569-0197 |
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 | A-S Medication Solutions LLC |
Substance Name | PHENAZOPYRIDINE HYDROCHLORIDE |
Strength Number | 200 |
Strength Unit | mg/1 |
Pharmaceutical Classes |