Mirtazapine
- Product NDC
- 71335-0532
- 11-digit product format
- 713350532
- Labeler code
- 71335
- Product ID
- 71335-0532_9bc7cb68-6916-43aa-b8d2-32a1477ca267
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076541
- Marketing category
- ANDA
- Marketing start
- 2004-04-22
- Marketing end
- 0000-00-00
- Substance
- MIRTAZAPINE
- Active strength
- 45 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0532-1 | 71335053201 | 30 TABLET in 1 BOTTLE (71335-0532-1) | 30 tablet | 2017-02-10 | 0000-00-00 | No | No | Current |
| 71335-0532-2 | 71335053202 | 90 TABLET in 1 BOTTLE (71335-0532-2) | 90 tablet | 2017-02-10 | 0000-00-00 | No | No | Current |
| 71335-0532-3 | 71335053203 | 60 TABLET in 1 BOTTLE (71335-0532-3) | 60 tablet | 2017-02-10 | 0000-00-00 | No | No | Current |
| 71335-0532-4 | 71335053204 | 28 TABLET in 1 BOTTLE (71335-0532-4) | 28 tablet | 2017-02-10 | 0000-00-00 | No | No | Current |