Mirtazapine
- Product NDC
- 55154-7141
- 11-digit product format
- 551547141
- Labeler code
- 55154
- Product ID
- 55154-7141_72b404cb-4708-4a42-ace4-e2fb3aa3a7de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA076921
- Marketing category
- ANDA
- Marketing start
- 2005-10-25
- Marketing end
- 0000-00-00
- Substance
- MIRTAZAPINE
- Active strength
- 30 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 55154-7141-0 | 55154714100 | 10 BLISTER PACK in 1 BAG (55154-7141-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2005-10-25 | 0000-00-00 | No | No | Current |