Product NDC: | 49614-174 |
Proprietary Name: | Allergy Relief |
Non Proprietary Name: | Loratadine |
Active Ingredient(s): | 5 mg/5mL & nbsp; Loratadine |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49614-174 |
Labeler Name: | Medicine Shoppe International Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA076805 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040820 |
Package NDC: | 49614-174-26 |
Package Description: | 1 BOTTLE in 1 CARTON (49614-174-26) > 120 mL in 1 BOTTLE |
NDC Code | 49614-174-26 |
Proprietary Name | Allergy Relief |
Package Description | 1 BOTTLE in 1 CARTON (49614-174-26) > 120 mL in 1 BOTTLE |
Product NDC | 49614-174 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Loratadine |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20040820 |
Marketing Category Name | ANDA |
Labeler Name | Medicine Shoppe International Inc |
Substance Name | LORATADINE |
Strength Number | 5 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |