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Mucus Relief D
Mucus Relief D - 41250-547-72 - (Guaifenesin, Pseudoephedrine HCl)
Drug Information of Mucus Relief D
| Product NDC: | 41250-547 |
| Proprietary Name: | Mucus Relief D |
| Non Proprietary Name: | Guaifenesin, Pseudoephedrine HCl |
| Active Ingredient(s): | 400; 40 mg/1; mg/1 & nbsp; Guaifenesin, Pseudoephedrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mucus Relief D
| Product NDC: | 41250-547 |
| Labeler Name: | Meijer |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20070126 |
Package Information of Mucus Relief D
| Package NDC: | 41250-547-72 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (41250-547-72) > 9 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Mucus Relief D
| NDC Code | 41250-547-72 |
| Proprietary Name | Mucus Relief D |
| Package Description | 3 BLISTER PACK in 1 CARTON (41250-547-72) > 9 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 41250-547 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin, Pseudoephedrine HCl |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20070126 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Meijer |
| Substance Name | GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 400; 40 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
