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Zodryl DEC 50
Zodryl DEC 50 - 43378-124-08 - (codeine phosphate, guaifenesin and pseudoephedrine hydrochloride)
Drug Information of Zodryl DEC 50
| Product NDC: | 43378-124 |
| Proprietary Name: | Zodryl DEC 50 |
| Non Proprietary Name: | codeine phosphate, guaifenesin and pseudoephedrine hydrochloride |
| Active Ingredient(s): | 5; 100; 30 mg/5mL; mg/5mL; mg/5mL & nbsp; codeine phosphate, guaifenesin and pseudoephedrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zodryl DEC 50
| Product NDC: | 43378-124 |
| Labeler Name: | CodaDose, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090824 |
Package Information of Zodryl DEC 50
| Package NDC: | 43378-124-08 |
| Package Description: | 236 mL in 1 BOTTLE, PLASTIC (43378-124-08) |
NDC Information of Zodryl DEC 50
| NDC Code | 43378-124-08 |
| Proprietary Name | Zodryl DEC 50 |
| Package Description | 236 mL in 1 BOTTLE, PLASTIC (43378-124-08) |
| Product NDC | 43378-124 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | codeine phosphate, guaifenesin and pseudoephedrine hydrochloride |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20090824 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CodaDose, Inc. |
| Substance Name | CODEINE PHOSPHATE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 5; 100; 30 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
