Nortriptyline Hydrochloride
- Product NDC
- 50090-0507
- 11-digit product format
- 500900507
- Labeler code
- 50090
- Product ID
- 50090-0507_2ce9368d-575c-419c-b257-5687673fe5a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075520
- Marketing category
- ANDA
- Marketing start
- 2000-05-08
- Marketing end
- 0000-00-00
- Substance
- NORTRIPTYLINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-0507 | NORTRIPTYLINE HYDROCHLORIDE CAPSULE [A-S MEDICATION SOLUTIONS] | 14 | Legacy NDC | 20240319_8409a9ed-5aea-45da-b71d-73fca8334e63.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0507-0 | 50090050700 | 30 CAPSULE in 1 BOTTLE (50090-0507-0) | 30 capsule | 2016-06-29 | 0000-00-00 | No | No | Current |
| 50090-0507-3 | 50090050703 | 90 CAPSULE in 1 BOTTLE (50090-0507-3) | 90 capsule | 2016-06-29 | 0000-00-00 | No | No | Current |