Loxapine
- Product NDC
- 10135-587
- 11-digit product format
- 101350587
- Labeler code
- 10135
- Product ID
- 10135-587_42bcc296-c005-416f-b0ad-2dccc0c8fe46
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Loxapine succinate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Marlex Pharmaceuticals Inc
- Application
- ANDA090695
- Marketing category
- ANDA
- Marketing start
- 2014-10-01
- Marketing end
- 0000-00-00
- Substance
- LOXAPINE SUCCINATE
- Active strength
- 25 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 10135-587-01 | Loxapine | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 10135-587-10 | Loxapine | 1000 in 1 BOTTLE | TABLET | 1000 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10135-587 | LOXAPINE (LOXAPINE SUCCINATE) TABLET [MARLEX PHARMACEUTICALS INC] | 1 | Legacy NDC, 2 package rows | 20160210_dee2537b-1bd8-42f6-990f-62359e646822.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10135-587-01 | 10135058701 | 100 in 1 BOTTLE | Historical |
| 10135-587-10 | 10135058710 | 1000 in 1 BOTTLE | Historical |