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Ephed Asthma
Ephed Asthma - 65193-320-46 - (ephedrine hydrochloride, guaifenesin)
Drug Information of Ephed Asthma
| Product NDC: | 65193-320 |
| Proprietary Name: | Ephed Asthma |
| Non Proprietary Name: | ephedrine hydrochloride, guaifenesin |
| Active Ingredient(s): | 25; 200 mg/1; mg/1 & nbsp; ephedrine hydrochloride, guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ephed Asthma
| Product NDC: | 65193-320 |
| Labeler Name: | Dickey Consumer Products DBA DMD |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111213 |
Package Information of Ephed Asthma
| Package NDC: | 65193-320-46 |
| Package Description: | 2 TABLET in 1 BLISTER PACK (65193-320-46) |
NDC Information of Ephed Asthma
| NDC Code | 65193-320-46 |
| Proprietary Name | Ephed Asthma |
| Package Description | 2 TABLET in 1 BLISTER PACK (65193-320-46) |
| Product NDC | 65193-320 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ephedrine hydrochloride, guaifenesin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111213 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dickey Consumer Products DBA DMD |
| Substance Name | EPHEDRINE HYDROCHLORIDE; GUAIFENESIN |
| Strength Number | 25; 200 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
