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NASOPEN
NASOPEN - 58809-578-02 - (Chlorcyclizine Hydrochloride, Pseudoephedrine Hydrochloride)
Drug Information of NASOPEN
| Product NDC: | 58809-578 |
| Proprietary Name: | NASOPEN |
| Non Proprietary Name: | Chlorcyclizine Hydrochloride, Pseudoephedrine Hydrochloride |
| Active Ingredient(s): | 9.375; 30 mg/5mL; mg/5mL & nbsp; Chlorcyclizine Hydrochloride, Pseudoephedrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NASOPEN
| Product NDC: | 58809-578 |
| Labeler Name: | GM Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110606 |
Package Information of NASOPEN
| Package NDC: | 58809-578-02 |
| Package Description: | 12 BOTTLE in 1 CARTON (58809-578-02) > 15 mL in 1 BOTTLE |
NDC Information of NASOPEN
| NDC Code | 58809-578-02 |
| Proprietary Name | NASOPEN |
| Package Description | 12 BOTTLE in 1 CARTON (58809-578-02) > 15 mL in 1 BOTTLE |
| Product NDC | 58809-578 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Chlorcyclizine Hydrochloride, Pseudoephedrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110606 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | GM Pharmaceuticals, Inc. |
| Substance Name | CHLORCYCLIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 9.375; 30 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
