Mirtazapine
- Product NDC
- 65084-476
- 11-digit product format
- 650840476
- Labeler code
- 65084
- Product ID
- 65084-476_bb02dd10-fb4e-08ca-e053-2995a90abcbf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- McKesson Corporation dba RX Pak
- Application
- ANDA077666
- Marketing category
- ANDA
- Marketing start
- 2007-08-22
- Marketing end
- 2021-08-31
- Substance
- MIRTAZAPINE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 65084-476-10 | 65084047610 | 10 BLISTER PACK in 1 BOX (65084-476-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2019-11-15 | 2021-08-31 | No | No | Current |