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PRIMATENE
PRIMATENE - 0573-2952-20 - (ephedrine hcl, guaifenesin)
Drug Information of PRIMATENE
| Product NDC: | 0573-2952 |
| Proprietary Name: | PRIMATENE |
| Non Proprietary Name: | ephedrine hcl, guaifenesin |
| Active Ingredient(s): | 12.5; 200 mg/1; mg/1 & nbsp; ephedrine hcl, guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PRIMATENE
| Product NDC: | 0573-2952 |
| Labeler Name: | Pfizer Consumer Healthcare |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20040106 |
Package Information of PRIMATENE
| Package NDC: | 0573-2952-20 |
| Package Description: | 5 BLISTER PACK in 1 CARTON (0573-2952-20) > 12 TABLET in 1 BLISTER PACK |
NDC Information of PRIMATENE
| NDC Code | 0573-2952-20 |
| Proprietary Name | PRIMATENE |
| Package Description | 5 BLISTER PACK in 1 CARTON (0573-2952-20) > 12 TABLET in 1 BLISTER PACK |
| Product NDC | 0573-2952 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ephedrine hcl, guaifenesin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20040106 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pfizer Consumer Healthcare |
| Substance Name | EPHEDRINE HYDROCHLORIDE; GUAIFENESIN |
| Strength Number | 12.5; 200 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
