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All day Allergy d
All day Allergy d - 0904-5831-12 - (Cetirizine HCl, Pseudoephedrine HCl)
Drug Information of All day Allergy d
| Product NDC: | 0904-5831 |
| Proprietary Name: | All day Allergy d |
| Non Proprietary Name: | Cetirizine HCl, Pseudoephedrine HCl |
| Active Ingredient(s): | 5; 120 mg/1; mg/1 & nbsp; Cetirizine HCl, Pseudoephedrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of All day Allergy d
| Product NDC: | 0904-5831 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077170 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080506 |
Package Information of All day Allergy d
| Package NDC: | 0904-5831-12 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (0904-5831-12) > 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of All day Allergy d
| NDC Code | 0904-5831-12 |
| Proprietary Name | All day Allergy d |
| Package Description | 2 BLISTER PACK in 1 CARTON (0904-5831-12) > 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 0904-5831 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cetirizine HCl, Pseudoephedrine HCl |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20080506 |
| Marketing Category Name | ANDA |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 5; 120 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
