Propofol
- Product NDC
- 72572-585
- 11-digit product format
- 725720585
- Labeler code
- 72572
- Product ID
- 72572-585_9db78e67-e664-4151-a8bf-46d2225bfce5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propofol
- Dosage form
- INJECTION, EMULSION
- Route
- INTRAVENOUS
- Labeler
- Civica, Inc.
- Application
- ANDA074848
- Marketing category
- ANDA
- Marketing start
- 2020-09-03
- Marketing end
- 0000-00-00
- Substance
- PROPOFOL
- Active strength
- 10 mg/mL
- Pharmacologic classes
- General Anesthesia [PE],General Anesthetic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72572-585-10 | 72572058510 | 10 VIAL, SINGLE-USE in 1 CARTON (72572-585-10) > 100 mL in 1 VIAL, SINGLE-USE (72572-585-01) | 2020-09-03 | 0000-00-00 | No | No | Current |