Sevoflurane
- Product NDC
- 72162-2245
- 11-digit product format
- 721622245
- Labeler code
- 72162
- Product ID
- 72162-2245_f512cb42-6831-4296-8716-6e366f6b05cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sevoflurane
- Dosage form
- LIQUID
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077867
- Marketing category
- ANDA
- Marketing start
- 2011-07-15
- Substance
- SEVOFLURANE
- Active strength
- 1 mL/mL
- Pharmacologic classes
- General Anesthesia [PE], General Anesthetic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 38LVP0K73A | SEVOFLURANE | 28523-86-6 | SEVOFLURANE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2245-2 | 72162224502 | 250 mL in 1 BOTTLE (72162-2245-2) | 250 ml | 2024-01-29 | No | No | Historical |