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Clofera
Clofera - 11528-140-16 - (Chlophedianol Hydrochloride and Pseudoephedrine Hydrochloride)
Drug Information of Clofera
| Product NDC: | 11528-140 |
| Proprietary Name: | Clofera |
| Non Proprietary Name: | Chlophedianol Hydrochloride and Pseudoephedrine Hydrochloride |
| Active Ingredient(s): | 12.5; 30 mg/5mL; mg/5mL & nbsp; Chlophedianol Hydrochloride and Pseudoephedrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clofera
| Product NDC: | 11528-140 |
| Labeler Name: | Centrix Pharmaceutical, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090814 |
Package Information of Clofera
| Package NDC: | 11528-140-16 |
| Package Description: | 473 mL in 1 BOTTLE (11528-140-16) |
NDC Information of Clofera
| NDC Code | 11528-140-16 |
| Proprietary Name | Clofera |
| Package Description | 473 mL in 1 BOTTLE (11528-140-16) |
| Product NDC | 11528-140 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Chlophedianol Hydrochloride and Pseudoephedrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20090814 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Centrix Pharmaceutical, Inc. |
| Substance Name | CHLOPHEDIANOL HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 12.5; 30 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
