Propofol
- Product NDC
- 52584-699
- 11-digit product format
- 525840699
- Labeler code
- 52584
- Product ID
- 52584-699_de4da48b-08c4-4c59-bf8e-c1afd3492bf0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propofol
- Dosage form
- INJECTION, EMULSION
- Route
- INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc
- Application
- ANDA077908
- Marketing category
- ANDA
- Marketing start
- 2014-08-21
- Marketing end
- 2023-02-01
- Substance
- PROPOFOL
- Active strength
- 10 mg/mL
- Pharmacologic classes
- General Anesthesia [PE],General Anesthetic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-699-33 | 52584069933 | 1 VIAL in 1 BAG (52584-699-33) > 50 mL in 1 VIAL | 1 vial | 2016-10-13 | 2023-02-01 | No | No | Current |