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Loratadine and Pseudoephedrine
Loratadine and Pseudoephedrine - 51660-724-69 - (loratadine and pseudoephedrine)
Drug Information of Loratadine and Pseudoephedrine
| Product NDC: | 51660-724 |
| Proprietary Name: | Loratadine and Pseudoephedrine |
| Non Proprietary Name: | loratadine and pseudoephedrine |
| Active Ingredient(s): | 10; 240 mg/1; mg/1 & nbsp; loratadine and pseudoephedrine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Loratadine and Pseudoephedrine
| Product NDC: | 51660-724 |
| Labeler Name: | Ohm Laboratories Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076557 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20041117 |
Package Information of Loratadine and Pseudoephedrine
| Package NDC: | 51660-724-69 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (51660-724-69) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of Loratadine and Pseudoephedrine
| NDC Code | 51660-724-69 |
| Proprietary Name | Loratadine and Pseudoephedrine |
| Package Description | 1 BLISTER PACK in 1 CARTON (51660-724-69) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 51660-724 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | loratadine and pseudoephedrine |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20041117 |
| Marketing Category Name | ANDA |
| Labeler Name | Ohm Laboratories Inc. |
| Substance Name | LORATADINE; PSEUDOEPHEDRINE SULFATE |
| Strength Number | 10; 240 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
