Epoprostenol Sodium
- Product NDC
- 0703-1985
- 11-digit product format
- 007031985
- Labeler code
- 0703
- Product ID
- 0703-1985_4198f1e6-f32f-4fc9-baf6-4982ef8e9685
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Epoprostenol Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Teva Parenteral Medicines, Inc.
- Application
- ANDA078396
- Marketing category
- ANDA
- Marketing start
- 2008-04-23
- Marketing end
- 0000-00-00
- Substance
- EPOPROSTENOL SODIUM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Prostacycline Vasodilator [EPC], Prostaglandins I [CS], Vasodilation [PE]
- 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 |
|---|
| 0703-1985-01 | 00703198501 | 1 VIAL in 1 CARTON (0703-1985-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 1 vial | 2008-04-23 | 0000-00-00 | No | No | Current |