Mirtazapine
- Product NDC
- 63629-5085
- 11-digit product format
- 636295085
- Labeler code
- 63629
- Product ID
- 63629-5085_b4fc13c9-e81b-42e5-9828-e8c7c06d197f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077376
- Marketing category
- ANDA
- Marketing start
- 2005-12-08
- Marketing end
- 0000-00-00
- Substance
- MIRTAZAPINE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63629-5085-1 | 63629508501 | 30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (63629-5085-1) | 2022-05-03 | 0000-00-00 | No | No | Current |
| 63629-5085-2 | 63629508502 | 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (63629-5085-2) | 2022-05-03 | 0000-00-00 | No | No | Current |
| 63629-5085-3 | 63629508503 | 29 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (63629-5085-3) | 2022-05-03 | 0000-00-00 | No | No | Current |