Mirtazapine
- Product NDC
- 63739-098
- 11-digit product format
- 637390098
- Labeler code
- 63739
- Product ID
- 63739-098_2bb25f3c-7005-6710-e063-6294a90a022c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA077666
- Marketing category
- ANDA
- Marketing start
- 2007-08-22
- Marketing end
- 2027-03-31
- Substance
- MIRTAZAPINE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Mirtazapine
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MIRTAZAPINE | 15 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | A051Q2099Q |
| Rxcui | 311725, 314111 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63739-098-10 | Mirtazapine | 10 in 1 BOX | TABLET, FILM COATED | 10 | | 11 |
| 63739-098-10 | Mirtazapine | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63739-098 | MIRTAZAPINE TABLET, FILM COATED [MCKESSON CORPORATION DBA SKY PACKAGING] | 11 | Current NDC, Legacy NDC, 2 package rows | 20250116_40c95daa-bbd5-48d9-97e4-c87f2c1f0fa5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-098-10 | 63739009810 | 10 BLISTER PACK in 1 BOX (63739-098-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2019-11-15 | 2027-03-31 | No | No | Current |