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Tyzine Pediatric
Tyzine Pediatric - 10337-477-15 - (TETRAHYDROZOLINE HYDROCHLORIDE)
Drug Information of Tyzine Pediatric
| Product NDC: | 10337-477 |
| Proprietary Name: | Tyzine Pediatric |
| Non Proprietary Name: | TETRAHYDROZOLINE HYDROCHLORIDE |
| Active Ingredient(s): | .5 mg/mL & nbsp; TETRAHYDROZOLINE HYDROCHLORIDE |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tyzine Pediatric
| Product NDC: | 10337-477 |
| Labeler Name: | PharmaDerm A division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA086576 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19791130 |
Package Information of Tyzine Pediatric
| Package NDC: | 10337-477-15 |
| Package Description: | 15 mL in 1 BOTTLE, DROPPER (10337-477-15) |
NDC Information of Tyzine Pediatric
| NDC Code | 10337-477-15 |
| Proprietary Name | Tyzine Pediatric |
| Package Description | 15 mL in 1 BOTTLE, DROPPER (10337-477-15) |
| Product NDC | 10337-477 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TETRAHYDROZOLINE HYDROCHLORIDE |
| Dosage Form Name | SOLUTION |
| Route Name | NASAL |
| Start Marketing Date | 19791130 |
| Marketing Category Name | ANDA |
| Labeler Name | PharmaDerm A division of Fougera Pharmaceuticals Inc. |
| Substance Name | TETRAHYDROZOLINE HYDROCHLORIDE |
| Strength Number | .5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
