Nortriptyline Hydrochloride
- Product NDC
- 50090-1323
- 11-digit product format
- 500901323
- Labeler code
- 50090
- Product ID
- 50090-1323_0cf7685e-79ea-4bd2-8a31-3907193eeb1a
- 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
- 50 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50090-1323 | NORTRIPTYLINE HYDROCHLORIDE CAPSULE [A-S MEDICATION SOLUTIONS] | 15 | Legacy NDC | 20240912_b675a15a-6e16-4921-924a-3f4d8c50918f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1323-0 | 50090132300 | 90 CAPSULE in 1 BOTTLE (50090-1323-0) | 90 capsule | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-1323-1 | 50090132301 | 30 CAPSULE in 1 BOTTLE (50090-1323-1) | 30 capsule | 2014-11-28 | 0000-00-00 | No | No | Current |