Mirtazapine
- Product NDC
- 70518-2582
- 11-digit product format
- 705182582
- Labeler code
- 70518
- Product ID
- 70518-2582_d6a98c6d-f3f3-cb0b-e053-2995a90a79ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076541
- Marketing category
- ANDA
- Marketing start
- 2020-02-17
- Marketing end
- 0000-00-00
- Substance
- MIRTAZAPINE
- Active strength
- 8 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2582-1 | 70518258201 | 30 POUCH in 1 BOX (70518-2582-1) > 1 TABLET in 1 POUCH (70518-2582-0) | 30 pouch | 2020-02-17 | 0000-00-00 | No | No | Current |