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sunmark loratadine d
sunmark loratadine d - 49348-183-47 - (Loratadine, Pseudoephedrine)
Drug Information of sunmark loratadine d
| Product NDC: | 49348-183 |
| Proprietary Name: | sunmark loratadine d |
| Non Proprietary Name: | Loratadine, Pseudoephedrine |
| Active Ingredient(s): | 5; 120 mg/1; mg/1 & nbsp; Loratadine, Pseudoephedrine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of sunmark loratadine d
| Product NDC: | 49348-183 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076050 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120306 |
Package Information of sunmark loratadine d
| Package NDC: | 49348-183-47 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (49348-183-47) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of sunmark loratadine d
| NDC Code | 49348-183-47 |
| Proprietary Name | sunmark loratadine d |
| Package Description | 2 BLISTER PACK in 1 CARTON (49348-183-47) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 49348-183 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loratadine, Pseudoephedrine |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120306 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | LORATADINE; PSEUDOEPHEDRINE SULFATE |
| Strength Number | 5; 120 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
