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De-Chlor
De-Chlor - 60258-521-16 - (Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, Chlorpheniramine Maleate)
Drug Information of De-Chlor
| Product NDC: | 60258-521 |
| Proprietary Name: | De-Chlor |
| Non Proprietary Name: | Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, Chlorpheniramine Maleate |
| Active Ingredient(s): | 2; 15; 10 mg/5mL; mg/5mL; mg/5mL & nbsp; Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, Chlorpheniramine Maleate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of De-Chlor
| Product NDC: | 60258-521 |
| Labeler Name: | Cypress Pharmaceutical, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110709 |
Package Information of De-Chlor
| Package NDC: | 60258-521-16 |
| Package Description: | 473 mL in 1 BOTTLE (60258-521-16) |
NDC Information of De-Chlor
| NDC Code | 60258-521-16 |
| Proprietary Name | De-Chlor |
| Package Description | 473 mL in 1 BOTTLE (60258-521-16) |
| Product NDC | 60258-521 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, Chlorpheniramine Maleate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110709 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Cypress Pharmaceutical, Inc. |
| Substance Name | CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 2; 15; 10 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
