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Allerest
Allerest - 63736-586-18 - (Chlorpheniramine Maleate and Phenylephrine Hydrochloride)
Drug Information of Allerest
| Product NDC: | 63736-586 |
| Proprietary Name: | Allerest |
| Non Proprietary Name: | Chlorpheniramine Maleate and Phenylephrine Hydrochloride |
| Active Ingredient(s): | 4; 10 mg/1; mg/1 & nbsp; Chlorpheniramine Maleate and Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Allerest
| Product NDC: | 63736-586 |
| Labeler Name: | Insight Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090731 |
Package Information of Allerest
| Package NDC: | 63736-586-18 |
| Package Description: | 1 BLISTER PACK in 1 BOX (63736-586-18) > 18 TABLET in 1 BLISTER PACK |
NDC Information of Allerest
| NDC Code | 63736-586-18 |
| Proprietary Name | Allerest |
| Package Description | 1 BLISTER PACK in 1 BOX (63736-586-18) > 18 TABLET in 1 BLISTER PACK |
| Product NDC | 63736-586 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Chlorpheniramine Maleate and Phenylephrine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090731 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Insight Pharmaceuticals |
| Substance Name | CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 4; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
