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THERAFLU
THERAFLU - 0067-6318-06 - (ACETAMINOPHEN, DIPHENHYDRAMINE, PHENYLEPHRINE)
Drug Information of THERAFLU
| Product NDC: | 0067-6318 |
| Proprietary Name: | THERAFLU |
| Non Proprietary Name: | ACETAMINOPHEN, DIPHENHYDRAMINE, PHENYLEPHRINE |
| Active Ingredient(s): | 650; 25; 10 mg/1; mg/1; mg/1 & nbsp; ACETAMINOPHEN, DIPHENHYDRAMINE, PHENYLEPHRINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of THERAFLU
| Product NDC: | 0067-6318 |
| Labeler Name: | Novartis Consumer Health, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090810 |
Package Information of THERAFLU
| Package NDC: | 0067-6318-06 |
| Package Description: | 6 POWDER, FOR SOLUTION in 1 CARTON (0067-6318-06) |
NDC Information of THERAFLU
| NDC Code | 0067-6318-06 |
| Proprietary Name | THERAFLU |
| Package Description | 6 POWDER, FOR SOLUTION in 1 CARTON (0067-6318-06) |
| Product NDC | 0067-6318 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOPHEN, DIPHENHYDRAMINE, PHENYLEPHRINE |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20090810 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Novartis Consumer Health, Inc. |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 650; 25; 10 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
