| Product NDC: | 10267-0064 |
| Proprietary Name: | Phenazo |
| Non Proprietary Name: | Phenozapyridine Hydrochloride |
| Active Ingredient(s): | 95 mg/1 & nbsp; Phenozapyridine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10267-0064 |
| Labeler Name: | Contract Pharmacal Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20111025 |
| Package NDC: | 10267-0064-3 |
| Package Description: | 15 POUCH in 1 CARTON (10267-0064-3) > 2 TABLET in 1 POUCH |
| NDC Code | 10267-0064-3 |
| Proprietary Name | Phenazo |
| Package Description | 15 POUCH in 1 CARTON (10267-0064-3) > 2 TABLET in 1 POUCH |
| Product NDC | 10267-0064 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Phenozapyridine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111025 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Contract Pharmacal Corp |
| Substance Name | PHENAZOPYRIDINE HYDROCHLORIDE |
| Strength Number | 95 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |