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Nasotuss
Nasotuss - 63717-276-99 - (Chlorcyclizine Hydrochloride, Codeine Phosphate, Phenylephrine Hydrochloride)
Drug Information of Nasotuss
| Product NDC: | 63717-276 |
| Proprietary Name: | Nasotuss |
| Non Proprietary Name: | Chlorcyclizine Hydrochloride, Codeine Phosphate, Phenylephrine Hydrochloride |
| Active Ingredient(s): | 25; 10; 10 mg/5mL; mg/5mL; mg/5mL & nbsp; Chlorcyclizine Hydrochloride, Codeine Phosphate, Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nasotuss
| Product NDC: | 63717-276 |
| Labeler Name: | Hawthorn Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101108 |
Package Information of Nasotuss
| Package NDC: | 63717-276-99 |
| Package Description: | 12 BOTTLE in 1 CARTON (63717-276-99) > 15 mL in 1 BOTTLE |
NDC Information of Nasotuss
| NDC Code | 63717-276-99 |
| Proprietary Name | Nasotuss |
| Package Description | 12 BOTTLE in 1 CARTON (63717-276-99) > 15 mL in 1 BOTTLE |
| Product NDC | 63717-276 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Chlorcyclizine Hydrochloride, Codeine Phosphate, Phenylephrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20101108 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Hawthorn Pharmaceuticals, Inc. |
| Substance Name | CHLORCYCLIZINE HYDROCHLORIDE; CODEINE PHOSPHATE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 25; 10; 10 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
