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Ultane
Ultane - 0074-4456-51 - (Sevoflurane)
Drug Information of Ultane
| Product NDC: | 0074-4456 |
| Proprietary Name: | Ultane |
| Non Proprietary Name: | Sevoflurane |
| Active Ingredient(s): | 250 mL/250mL & nbsp; Sevoflurane |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ultane
| Product NDC: | 0074-4456 |
| Labeler Name: | AbbVie Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020478 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19950607 |
Package Information of Ultane
| Package NDC: | 0074-4456-51 |
| Package Description: | 250 mL in 1 BOTTLE, PLASTIC (0074-4456-51) |
NDC Information of Ultane
| NDC Code | 0074-4456-51 |
| Proprietary Name | Ultane |
| Package Description | 250 mL in 1 BOTTLE, PLASTIC (0074-4456-51) |
| Product NDC | 0074-4456 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sevoflurane |
| Dosage Form Name | LIQUID |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 19950607 |
| Marketing Category Name | NDA |
| Labeler Name | AbbVie Inc. |
| Substance Name | SEVOFLURANE |
| Strength Number | 250 |
| Strength Unit | mL/250mL |
| Pharmaceutical Classes | General Anesthesia [PE],General Anesthetic [EPC] |
