Product NDC: | 37205-321 |
Proprietary Name: | Leader Heartburn Relief |
Non Proprietary Name: | Cimetidine |
Active Ingredient(s): | 200 mg/1 & nbsp; Cimetidine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37205-321 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA075285 |
Marketing Category: | ANDA |
Start Marketing Date: | 20000204 |
Package NDC: | 37205-321-65 |
Package Description: | 1 BOTTLE in 1 CARTON (37205-321-65) > 30 TABLET in 1 BOTTLE |
NDC Code | 37205-321-65 |
Proprietary Name | Leader Heartburn Relief |
Package Description | 1 BOTTLE in 1 CARTON (37205-321-65) > 30 TABLET in 1 BOTTLE |
Product NDC | 37205-321 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Cimetidine |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20000204 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | CIMETIDINE |
Strength Number | 200 |
Strength Unit | mg/1 |
Pharmaceutical Classes |