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smart sense acid reducer
smart sense acid reducer - 49738-950-62 - (Ranitidine)
Drug Information of smart sense acid reducer
| Product NDC: | 49738-950 |
| Proprietary Name: | smart sense acid reducer |
| 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) |
Labeler Information of smart sense acid reducer
| Product NDC: | 49738-950 |
| Labeler Name: | Kmart Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA091429 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111122 |
Package Information of smart sense acid reducer
| Package NDC: | 49738-950-62 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (49738-950-62) > 8 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of smart sense acid reducer
| NDC Code | 49738-950-62 |
| Proprietary Name | smart sense acid reducer |
| Package Description | 3 BLISTER PACK in 1 CARTON (49738-950-62) > 8 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 49738-950 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ranitidine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20111122 |
| Marketing Category Name | ANDA |
| Labeler Name | Kmart Corporation |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
