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TUMS
TUMS - 0135-0562-01 - (calcium carbonate)
Drug Information of TUMS
| Product NDC: | 0135-0562 |
| 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) |
Labeler Information of TUMS
| Product NDC: | 0135-0562 |
| Labeler Name: | GlaxoSmithKline Consumer Heathcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130415 |
Package Information of TUMS
| Package NDC: | 0135-0562-01 |
| Package Description: | 1 KIT in 1 CARTON (0135-0562-01) * 96 TABLET, CHEWABLE in 1 BOTTLE * 8 TABLET, CHEWABLE in 1 PACKAGE |
NDC Information of TUMS
| NDC Code | 0135-0562-01 |
| Proprietary Name | TUMS |
| Package Description | 1 KIT in 1 CARTON (0135-0562-01) * 96 TABLET, CHEWABLE in 1 BOTTLE * 8 TABLET, CHEWABLE in 1 PACKAGE |
| Product NDC | 0135-0562 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | calcium carbonate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20130415 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | GlaxoSmithKline Consumer Heathcare LP |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
