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rexall heartburn relief
rexall heartburn relief - 55910-950-62 - (Ranitidine)
Drug Information of rexall heartburn relief
| Product NDC: | 55910-950 |
| Proprietary Name: | rexall heartburn relief |
| 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 rexall heartburn relief
| Product NDC: | 55910-950 |
| Labeler Name: | Dolgencorp, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA091429 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111003 |
Package Information of rexall heartburn relief
| Package NDC: | 55910-950-62 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (55910-950-62) > 8 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of rexall heartburn relief
| NDC Code | 55910-950-62 |
| Proprietary Name | rexall heartburn relief |
| Package Description | 3 BLISTER PACK in 1 CARTON (55910-950-62) > 8 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 55910-950 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ranitidine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20111003 |
| Marketing Category Name | ANDA |
| Labeler Name | Dolgencorp, LLC |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
