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ConRx - 68737-227-11 - (Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride)
Drug Information of ConRx
| Product NDC: | 68737-227 |
| Proprietary Name: | ConRx |
| Non Proprietary Name: | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride |
| Active Ingredient(s): | 325; 10; 200; 5 mg/1; mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ConRx
| Product NDC: | 68737-227 |
| Labeler Name: | Eagle Distributors,Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120710 |
Package Information of ConRx
| Package NDC: | 68737-227-11 |
| Package Description: | 50 POUCH in 1 BOX (68737-227-11) > 2 TABLET in 1 POUCH |
NDC Information of ConRx
| NDC Code | 68737-227-11 |
| Proprietary Name | ConRx |
| Package Description | 50 POUCH in 1 BOX (68737-227-11) > 2 TABLET in 1 POUCH |
| Product NDC | 68737-227 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120710 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Eagle Distributors,Inc. |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 10; 200; 5 |
| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
