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Moore Medical Loratadine
Moore Medical Loratadine - 55670-478-50 - (Loratadine)
Drug Information of Moore Medical Loratadine
| Product NDC: | 55670-478 |
| Proprietary Name: | Moore Medical Loratadine |
| Non Proprietary Name: | Loratadine |
| Active Ingredient(s): | 10 mg/1 & nbsp; Loratadine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Moore Medical Loratadine
| Product NDC: | 55670-478 |
| Labeler Name: | Moore Medical LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076134 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081230 |
Package Information of Moore Medical Loratadine
| Package NDC: | 55670-478-50 |
| Package Description: | 50 PACKET in 1 BOX, UNIT-DOSE (55670-478-50) > 1 TABLET, FILM COATED in 1 PACKET (55670-478-46) |
NDC Information of Moore Medical Loratadine
| NDC Code | 55670-478-50 |
| Proprietary Name | Moore Medical Loratadine |
| Package Description | 50 PACKET in 1 BOX, UNIT-DOSE (55670-478-50) > 1 TABLET, FILM COATED in 1 PACKET (55670-478-46) |
| Product NDC | 55670-478 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loratadine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20081230 |
| Marketing Category Name | ANDA |
| Labeler Name | Moore Medical LLC |
| Substance Name | LORATADINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
