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HELIDAC Therapy
HELIDAC Therapy - 65483-495-14 - (bismuth subsalicylate, metronidazole and tetracycline hydrochloride)
Drug Information of HELIDAC Therapy
| Product NDC: | 65483-495 |
| Proprietary Name: | HELIDAC Therapy |
| Non Proprietary Name: | bismuth subsalicylate, metronidazole and tetracycline hydrochloride |
| Active Ingredient(s): | & nbsp; bismuth subsalicylate, metronidazole and tetracycline hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HELIDAC Therapy
| Product NDC: | 65483-495 |
| Labeler Name: | Prometheus Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050719 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19960815 |
Package Information of HELIDAC Therapy
| Package NDC: | 65483-495-14 |
| Package Description: | 14 BLISTER PACK in 1 CARTON (65483-495-14) > 1 KIT in 1 BLISTER PACK |
NDC Information of HELIDAC Therapy
| NDC Code | 65483-495-14 |
| Proprietary Name | HELIDAC Therapy |
| Package Description | 14 BLISTER PACK in 1 CARTON (65483-495-14) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 65483-495 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | bismuth subsalicylate, metronidazole and tetracycline hydrochloride |
| Dosage Form Name | KIT |
| Route Name | ORAL |
| Start Marketing Date | 19960815 |
| Marketing Category Name | NDA |
| Labeler Name | Prometheus Laboratories Inc. |
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