Nortriptyline Hydrochloride
- Product NDC
- 68788-8158
- 11-digit product format
- 687888158
- Labeler code
- 68788
- Product ID
- 68788-8158_7b346652-831b-4a09-ab8d-7d5a548d3348
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA073556
- Marketing category
- ANDA
- Marketing start
- 2022-03-24
- Marketing end
- 0000-00-00
- Substance
- NORTRIPTYLINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-8158 | NORTRIPTYLINE HYDROCHLORIDE CAPSULE [PREFERRED PHARMACEUTICALS INC.] | 3 | Legacy NDC | 20240725_7b346652-831b-4a09-ab8d-7d5a548d3348.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8158-3 | 68788815803 | 30 CAPSULE in 1 BOTTLE, PLASTIC (68788-8158-3) | 30 capsule | 2022-03-24 | 0000-00-00 | No | No | Current |