Mirtazapine
- Product NDC
- 16714-708
- 11-digit product format
- 167140708
- Labeler code
- 16714
- Product ID
- 16714-708_0506d20e-0f1c-4bd5-a298-383279478f20
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northstar Rx LLC
- Application
- ANDA076541
- Marketing category
- ANDA
- Marketing start
- 2017-04-11
- Marketing end
- 2021-04-30
- Substance
- MIRTAZAPINE
- Active strength
- 30 mg/1
- 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 |
|---|
| 16714-708-01 | 16714070801 | 30 TABLET in 1 BOTTLE (16714-708-01) | 30 tablet | 2017-04-11 | 2021-03-31 | No | No | Current |