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ED BRON GP
ED BRON GP - 0485-0208-16 - (GUAIFENESIN and PHENYLEPHRINE)
Drug Information of ED BRON GP
| Product NDC: | 0485-0208 |
| Proprietary Name: | ED BRON GP |
| Non Proprietary Name: | GUAIFENESIN and PHENYLEPHRINE |
| Active Ingredient(s): | 100; 5 mg/5mL; mg/5mL & nbsp; GUAIFENESIN and PHENYLEPHRINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ED BRON GP
| Product NDC: | 0485-0208 |
| Labeler Name: | EDWARDS PHARMACEUTICALS, INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120601 |
Package Information of ED BRON GP
| Package NDC: | 0485-0208-16 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (0485-0208-16) |
NDC Information of ED BRON GP
| NDC Code | 0485-0208-16 |
| Proprietary Name | ED BRON GP |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (0485-0208-16) |
| Product NDC | 0485-0208 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | GUAIFENESIN and PHENYLEPHRINE |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120601 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | EDWARDS PHARMACEUTICALS, INC. |
| Substance Name | GUAIFENESIN; PHENYLEPHRINE |
| Strength Number | 100; 5 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
