Product NDC: | 0135-0556 |
Proprietary Name: | Tums |
Non Proprietary Name: | calcium carbonate |
Active Ingredient(s): | & nbsp; calcium carbonate |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0135-0556 |
Labeler Name: | GlaxoSmithKline Consumer Heathcare LP |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130412 |
Package NDC: | 0135-0556-01 |
Package Description: | 1 KIT in 1 CARTON (0135-0556-01) * 72 TABLET, CHEWABLE in 1 BOTTLE * 8 TABLET, CHEWABLE in 1 BOTTLE |
NDC Code | 0135-0556-01 |
Proprietary Name | Tums |
Package Description | 1 KIT in 1 CARTON (0135-0556-01) * 72 TABLET, CHEWABLE in 1 BOTTLE * 8 TABLET, CHEWABLE in 1 BOTTLE |
Product NDC | 0135-0556 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | calcium carbonate |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20130412 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | GlaxoSmithKline Consumer Heathcare LP |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |