Nortriptyline Hydrochloride
- Product NDC
- 58118-4002
- 11-digit product format
- 581184002
- Labeler code
- 58118
- Product ID
- 58118-4002_ab5c851c-ce5a-d8f1-e053-2995a90a6a42
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale, LLC
- 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 |
|---|
| 58118-4002 | NORTRIPTYLINE HYDROCHLORIDE CAPSULE [CLINICAL SOLUTIONS WHOLESALE, LLC] | 7 | Legacy NDC | 20200727_424b48cd-e162-4291-bc0a-c047cb59b53c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58118-4002-8 | 58118400208 | 30 CAPSULE in 1 BLISTER PACK (58118-4002-8) | 30 capsule | 2016-10-12 | 0000-00-00 | No | No | Current |