Product NDC: | 16477-820 |
Proprietary Name: | Dallergy |
Non Proprietary Name: | Chlorcyclizine Hydrochloride, Phenylephrine Hydrochloride |
Active Ingredient(s): | 12.5; 5 mg/5mL; mg/5mL & nbsp; Chlorcyclizine Hydrochloride, Phenylephrine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | SYRUP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16477-820 |
Labeler Name: | Laser Pharmaceuticals, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20111018 |
Package NDC: | 16477-820-01 |
Package Description: | 473 mL in 1 BOTTLE (16477-820-01) |
NDC Code | 16477-820-01 |
Proprietary Name | Dallergy |
Package Description | 473 mL in 1 BOTTLE (16477-820-01) |
Product NDC | 16477-820 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Chlorcyclizine Hydrochloride, Phenylephrine Hydrochloride |
Dosage Form Name | SYRUP |
Route Name | ORAL |
Start Marketing Date | 20111018 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Laser Pharmaceuticals, LLC |
Substance Name | CHLORCYCLIZINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 12.5; 5 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes |