Propofol
- Product NDC
- 50090-4569
- 11-digit product format
- 500904569
- Labeler code
- 50090
- Product ID
- 50090-4569_a81abb0a-495a-4b53-9d04-8b8d1f973a29
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propofol
- Dosage form
- INJECTION, EMULSION
- Route
- INTRAVENOUS
- Labeler
- A-S Medication Solutions
- Application
- ANDA205307
- Marketing category
- ANDA
- Marketing start
- 2016-01-07
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4569 | PROPOFOL INJECTION, EMULSION [A-S MEDICATION SOLUTIONS] | 4 | Legacy NDC | 20210417_475de1f2-9b88-455a-ba3c-48e96083c056.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4569-1 | 50090456901 | 50 mL in 1 VIAL (50090-4569-1) | 50 ml | 2019-09-27 | 0000-00-00 | No | No | Current |