Propofol
- Product NDC
- 70518-3256
- 11-digit product format
- 705183256
- Labeler code
- 70518
- Product ID
- 70518-3256_cf41f987-2670-ecc3-e053-2995a90ae98b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propofol
- Dosage form
- INJECTION, EMULSION
- Route
- INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074848
- Marketing category
- ANDA
- Marketing start
- 2021-10-25
- 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3256-0 | 70518325600 | 10 VIAL, SINGLE-USE in 1 CARTON (70518-3256-0) > 20 mL in 1 VIAL, SINGLE-USE | 2021-10-25 | 0000-00-00 | No | No | Current |