WILZIN
- Product NDC
- 57844-376
- 11-digit product format
- 578440376
- Labeler code
- 57844
- Product ID
- 57844-376_04cae233-849e-4072-a8a7-4b15ae9ac492
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zinc acetate dihydrate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Marketing category
- UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
- Marketing start
- 2020-12-15
- Marketing end
- 2022-10-31
- Substance
- ZINC ACETATE
- Active strength
- 25 mg/1
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57844-376-25 | 57844037625 | 250 CAPSULE in 1 BOTTLE (57844-376-25) | 250 capsule | 2020-12-15 | 2022-10-31 | No | No | Current |