Torsemide
- Product NDC
- 0517-0771
- 11-digit product format
- 005170771
- Labeler code
- 0517
- Product ID
- 0517-0771_d81b99eb-cb6d-4644-941e-12e671910a29
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Torsemide
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- American Regent, Inc.
- Application
- ANDA090656
- Marketing category
- ANDA
- Marketing start
- 2010-05-26
- Marketing end
- 0000-00-00
- Substance
- TORSEMIDE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0517-0771-10 | 00517077110 | 10 VIAL, SINGLE-DOSE in 1 CARTON (0517-0771-10) > 5 mL in 1 VIAL, SINGLE-DOSE (0517-0771-01) | 2010-05-26 | 0000-00-00 | No | No | Current |