PROPOFOL
- Product NDC
- 0404-9943
- 11-digit product format
- 004049943
- Labeler code
- 0404
- Product ID
- 0404-9943_c5524e9d-ded6-4074-9637-9a28dc638933
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propofol
- Dosage form
- INJECTION, EMULSION
- Route
- INTRAVENOUS
- Labeler
- Henry Schein, Inc.
- Application
- ANDA205307
- Marketing category
- ANDA
- Marketing start
- 2022-01-13
- 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
- 2023-12-31
- 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 |
|---|
| 0404-9943-50 | 00404994350 | 1 VIAL in 1 BAG (0404-9943-50) > 50 mL in 1 VIAL | 1 vial | 2022-01-13 | 0000-00-00 | No | No | Current |