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sunmark cold and allergy
sunmark cold and allergy - 49348-715-04 - (Chlorpheniramine maleate, Phenylephrine HCl)
Drug Information of sunmark cold and allergy
| Product NDC: | 49348-715 |
| Proprietary Name: | sunmark cold and allergy |
| Non Proprietary Name: | Chlorpheniramine maleate, Phenylephrine HCl |
| Active Ingredient(s): | 4; 10 mg/1; mg/1 & nbsp; Chlorpheniramine maleate, Phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of sunmark cold and allergy
| Product NDC: | 49348-715 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20060922 |
Package Information of sunmark cold and allergy
| Package NDC: | 49348-715-04 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (49348-715-04) > 24 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of sunmark cold and allergy
| NDC Code | 49348-715-04 |
| Proprietary Name | sunmark cold and allergy |
| Package Description | 1 BLISTER PACK in 1 CARTON (49348-715-04) > 24 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 49348-715 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Chlorpheniramine maleate, Phenylephrine HCl |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20060922 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McKesson |
| Substance Name | CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 4; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
