mirtazapine
- Product NDC
- 70771-1073
- 11-digit product format
- 707711073
- Labeler code
- 70771
- Product ID
- 70771-1073_6c3c6185-e272-46c5-85da-24a457efc412
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- mirtazapine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Cadila Healthcare Limited
- Application
- ANDA205798
- Marketing category
- ANDA
- Marketing start
- 2017-07-20
- Marketing end
- 0000-00-00
- Substance
- MIRTAZAPINE
- Active strength
- 30 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 70771-1073-4 | 70771107304 | 30 TABLET, ORALLY DISINTEGRATING in 1 CARTON (70771-1073-4) | 2017-07-20 | 0000-00-00 | No | No | Current |