MIRTAZAPINE
- Product NDC
- 61919-154
- 11-digit product format
- 619190154
- Labeler code
- 61919
- Product ID
- 61919-154_3fa07d63-34aa-0486-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MIRTAZAPINE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA077666
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- Marketing end
- 0000-00-00
- Substance
- MIRTAZAPINE
- Active strength
- 30 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-154-30 | MIRTAZAPINE | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-154 | MIRTAZAPINE TABLET, FILM COATED [DIRECT RX] | 5 | Legacy NDC, 1 package rows | 20230422_c4b9346d-534e-4987-bdac-7b06bda05cba.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 61919-154-30 | 61919015430 | 30 in 1 BOTTLE | Historical |