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MucaphEd
MucaphEd - 0485-0250-01 - (GUAIFENESIN and PHENYLEPHRINE HYDROCHLORIDE)
Drug Information of MucaphEd
| Product NDC: | 0485-0250 |
| Proprietary Name: | MucaphEd |
| Non Proprietary Name: | GUAIFENESIN and PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient(s): | 400; 10 mg/1; mg/1 & nbsp; GUAIFENESIN and PHENYLEPHRINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MucaphEd
| Product NDC: | 0485-0250 |
| Labeler Name: | EDWARDS PHARMACEUTICALS, INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120911 |
Package Information of MucaphEd
| Package NDC: | 0485-0250-01 |
| Package Description: | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (0485-0250-01) |
NDC Information of MucaphEd
| NDC Code | 0485-0250-01 |
| Proprietary Name | MucaphEd |
| Package Description | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (0485-0250-01) |
| Product NDC | 0485-0250 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | GUAIFENESIN and PHENYLEPHRINE HYDROCHLORIDE |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120911 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | EDWARDS PHARMACEUTICALS, INC. |
| Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 400; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
