Product NDC: | 36800-950 |
Proprietary Name: | topcare heartburn relief 150 |
Non Proprietary Name: | Ranitidine |
Active Ingredient(s): | 150 mg/1 & nbsp; Ranitidine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 36800-950 |
Labeler Name: | Topco Associates LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA091429 |
Marketing Category: | ANDA |
Start Marketing Date: | 20111010 |
Package NDC: | 36800-950-05 |
Package Description: | 1 BLISTER PACK in 1 CARTON (36800-950-05) > 32 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Code | 36800-950-05 |
Proprietary Name | topcare heartburn relief 150 |
Package Description | 1 BLISTER PACK in 1 CARTON (36800-950-05) > 32 TABLET, FILM COATED in 1 BLISTER PACK |
Product NDC | 36800-950 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ranitidine |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20111010 |
Marketing Category Name | ANDA |
Labeler Name | Topco Associates LLC |
Substance Name | RANITIDINE HYDROCHLORIDE |
Strength Number | 150 |
Strength Unit | mg/1 |
Pharmaceutical Classes |