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Phenazopyridine Hydrochloride
Phenazopyridine Hydrochloride - 21695-301-16 - (Phenazopyridine)
Drug Information of Phenazopyridine Hydrochloride
| Product NDC: | 21695-301 |
| Proprietary Name: | Phenazopyridine Hydrochloride |
| Non Proprietary Name: | Phenazopyridine |
| Active Ingredient(s): | 200 mg/1 & nbsp; Phenazopyridine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phenazopyridine Hydrochloride
| Product NDC: | 21695-301 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110201 |
Package Information of Phenazopyridine Hydrochloride
| Package NDC: | 21695-301-16 |
| Package Description: | 16 TABLET in 1 BOTTLE (21695-301-16) |
NDC Information of Phenazopyridine Hydrochloride
| NDC Code | 21695-301-16 |
| Proprietary Name | Phenazopyridine Hydrochloride |
| Package Description | 16 TABLET in 1 BOTTLE (21695-301-16) |
| Product NDC | 21695-301 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenazopyridine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110201 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | PHENAZOPYRIDINE HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
