Zinc Sulfate
- Product NDC
- 0517-8105
- 11-digit product format
- 005178105
- Labeler code
- 0517
- Product ID
- 0517-8105_0ec7e3c8-375e-48fb-898d-f89057995aa0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zinc Sulfate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- American Regent, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1990-09-30
- Marketing end
- 2021-02-28
- Substance
- ZINC SULFATE ANHYDROUS
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC],Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0517-8105-25 | 00517810525 | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-8105-25) > 5 mL in 1 VIAL, SINGLE-DOSE | 1990-09-30 | 2021-02-28 | No | No | Current |