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leader acid control
leader acid control - 37205-845-62 - (Ranitidine)
Drug Information of leader acid control
| Product NDC: | 37205-845 |
| Proprietary Name: | leader acid control |
| 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 leader acid control
| Product NDC: | 37205-845 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA091429 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111111 |
Package Information of leader acid control
| Package NDC: | 37205-845-62 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (37205-845-62) > 8 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of leader acid control
| NDC Code | 37205-845-62 |
| Proprietary Name | leader acid control |
| Package Description | 3 BLISTER PACK in 1 CARTON (37205-845-62) > 8 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 37205-845 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ranitidine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20111111 |
| Marketing Category Name | ANDA |
| Labeler Name | Cardinal Health |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
