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Ventavis
Ventavis - 66215-303-30 - (iloprost)
Drug Information of Ventavis
| Product NDC: | 66215-303 |
| Proprietary Name: | Ventavis |
| Non Proprietary Name: | iloprost |
| Active Ingredient(s): | .02 mg/mL & nbsp; iloprost |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ventavis
| Product NDC: | 66215-303 |
| Labeler Name: | Actelion Pharmaceuticals US, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021779 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090824 |
Package Information of Ventavis
| Package NDC: | 66215-303-30 |
| Package Description: | 30 AMPULE in 1 CARTON (66215-303-30) > 1 mL in 1 AMPULE (66215-303-00) |
NDC Information of Ventavis
| NDC Code | 66215-303-30 |
| Proprietary Name | Ventavis |
| Package Description | 30 AMPULE in 1 CARTON (66215-303-30) > 1 mL in 1 AMPULE (66215-303-00) |
| Product NDC | 66215-303 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | iloprost |
| Dosage Form Name | SOLUTION |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20090824 |
| Marketing Category Name | NDA |
| Labeler Name | Actelion Pharmaceuticals US, Inc. |
| Substance Name | ILOPROST |
| Strength Number | .02 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Prostacycline [EPC],Prostaglandins I [Chemical/Ingredient] |
