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Effervescent Cold Relief
Effervescent Cold Relief - 50201-0246-1 - (ASPIRIN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE BITARTRATE)
Drug Information of Effervescent Cold Relief
| Product NDC: | 50201-0246 |
| Proprietary Name: | Effervescent Cold Relief |
| Non Proprietary Name: | ASPIRIN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE BITARTRATE |
| Active Ingredient(s): | 325; 2; 7.8 mg/1; mg/1; mg/1 & nbsp; ASPIRIN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE BITARTRATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EFFERVESCENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Effervescent Cold Relief
| Product NDC: | 50201-0246 |
| Labeler Name: | Tower Laboratories Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100701 |
Package Information of Effervescent Cold Relief
| Package NDC: | 50201-0246-1 |
| Package Description: | 2 TABLET, EFFERVESCENT in 1 POUCH (50201-0246-1) |
NDC Information of Effervescent Cold Relief
| NDC Code | 50201-0246-1 |
| Proprietary Name | Effervescent Cold Relief |
| Package Description | 2 TABLET, EFFERVESCENT in 1 POUCH (50201-0246-1) |
| Product NDC | 50201-0246 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ASPIRIN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE BITARTRATE |
| Dosage Form Name | TABLET, EFFERVESCENT |
| Route Name | ORAL |
| Start Marketing Date | 20100701 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Tower Laboratories Ltd |
| Substance Name | ASPIRIN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE BITARTRATE |
| Strength Number | 325; 2; 7.8 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
