Product NDC: | 0113-0612 |
Proprietary Name: | good sense allergy relief |
Non Proprietary Name: | Loratadine |
Active Ingredient(s): | 10 mg/1 & nbsp; Loratadine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0113-0612 |
Labeler Name: | L Perrigo Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA076301 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040921 |
Package NDC: | 0113-0612-60 |
Package Description: | 2 BLISTER PACK in 1 CARTON (0113-0612-60) > 10 TABLET in 1 BLISTER PACK |
NDC Code | 0113-0612-60 |
Proprietary Name | good sense allergy relief |
Package Description | 2 BLISTER PACK in 1 CARTON (0113-0612-60) > 10 TABLET in 1 BLISTER PACK |
Product NDC | 0113-0612 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Loratadine |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20040921 |
Marketing Category Name | ANDA |
Labeler Name | L Perrigo Company |
Substance Name | LORATADINE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes |