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Norel AD
Norel AD - 52747-475-70 - (acetaminophen, chlorpheniramine maleate, and phenylephrine HCl)
Drug Information of Norel AD
| Product NDC: | 52747-475 |
| Proprietary Name: | Norel AD |
| Non Proprietary Name: | acetaminophen, chlorpheniramine maleate, and phenylephrine HCl |
| Active Ingredient(s): | 325; 4; 10 mg/1; mg/1; mg/1 & nbsp; acetaminophen, chlorpheniramine maleate, and phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, MULTILAYER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Norel AD
| Product NDC: | 52747-475 |
| Labeler Name: | US Pharmaceutical Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120427 |
Package Information of Norel AD
| Package NDC: | 52747-475-70 |
| Package Description: | 20 TABLET, MULTILAYER in 1 BOTTLE (52747-475-70) |
NDC Information of Norel AD
| NDC Code | 52747-475-70 |
| Proprietary Name | Norel AD |
| Package Description | 20 TABLET, MULTILAYER in 1 BOTTLE (52747-475-70) |
| Product NDC | 52747-475 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen, chlorpheniramine maleate, and phenylephrine HCl |
| Dosage Form Name | TABLET, MULTILAYER |
| Route Name | ORAL |
| Start Marketing Date | 20120427 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | US Pharmaceutical Corporation |
| Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 4; 10 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
