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ALAVERT ALLERGY SINUS D-12
ALAVERT ALLERGY SINUS D-12 - 0573-2660-12 - (loratadine, pseudoephedrine sulfate)
Drug Information of ALAVERT ALLERGY SINUS D-12
| Product NDC: | 0573-2660 |
| Proprietary Name: | ALAVERT ALLERGY SINUS D-12 |
| Non Proprietary Name: | loratadine, pseudoephedrine sulfate |
| Active Ingredient(s): | 5; 120 mg/1; mg/1 & nbsp; loratadine, pseudoephedrine sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ALAVERT ALLERGY SINUS D-12
| Product NDC: | 0573-2660 |
| Labeler Name: | Wyeth Consumer Healthcare |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076050 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040130 |
Package Information of ALAVERT ALLERGY SINUS D-12
| Package NDC: | 0573-2660-12 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (0573-2660-12) > 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of ALAVERT ALLERGY SINUS D-12
| NDC Code | 0573-2660-12 |
| Proprietary Name | ALAVERT ALLERGY SINUS D-12 |
| Package Description | 2 BLISTER PACK in 1 CARTON (0573-2660-12) > 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 0573-2660 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | loratadine, pseudoephedrine sulfate |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20040130 |
| Marketing Category Name | ANDA |
| Labeler Name | Wyeth Consumer Healthcare |
| Substance Name | LORATADINE; PSEUDOEPHEDRINE SULFATE |
| Strength Number | 5; 120 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
