Manganese Sulfate
- Product NDC
- 0517-6410
- 11-digit product format
- 005176410
- Labeler code
- 0517
- Product ID
- 0517-6410_4022027e-31f8-452c-8f4a-b8d47b37e86d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Manganese Sulfate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- American Regent, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1990-09-30
- Marketing end
- 0000-00-00
- Substance
- MANGANESE SULFATE
- Active strength
- 0 mg/mL
- Pharmacologic classes
- Magnetic Resonance Contrast Activity [MoA],Paramagnetic Contrast Agent [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 |
|---|
| 0517-6410-25 | 00517641025 | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-6410-25) > 10 mL in 1 VIAL, SINGLE-DOSE | 1990-09-30 | 0000-00-00 | No | No | Current |