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SUNMARK ALLERGY RELIEF
SUNMARK ALLERGY RELIEF - 49348-637-04 - (Loratadine)
Drug Information of SUNMARK ALLERGY RELIEF
| Product NDC: | 49348-637 |
| Proprietary Name: | SUNMARK ALLERGY RELIEF |
| Non Proprietary Name: | Loratadine |
| Active Ingredient(s): | 10 mg/1 & nbsp; Loratadine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUNMARK ALLERGY RELIEF
| Product NDC: | 49348-637 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075990 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040202 |
Package Information of SUNMARK ALLERGY RELIEF
| Package NDC: | 49348-637-04 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (49348-637-04) > 12 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
NDC Information of SUNMARK ALLERGY RELIEF
| NDC Code | 49348-637-04 |
| Proprietary Name | SUNMARK ALLERGY RELIEF |
| Package Description | 2 BLISTER PACK in 1 CARTON (49348-637-04) > 12 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
| Product NDC | 49348-637 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loratadine |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20040202 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | LORATADINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
