Nortriptyline Hydrochloride
- Product NDC
- 50268-605
- 11-digit product format
- 502680605
- Labeler code
- 50268
- Product ID
- 50268-605_d5dea230-261a-f238-e053-2a95a90a5afd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA075520
- Marketing category
- ANDA
- Marketing start
- 2017-03-14
- 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
- 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 |
|---|
| 50268-605 | NORTRIPTYLINE HYDROCHLORIDE CAPSULE [AVPAK] | 4 | Legacy NDC | 20240110_1e0d6f54-c073-4d4c-a614-82b4da8364eb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50268-605-15 | 50268060515 | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-605-15) > 1 CAPSULE in 1 BLISTER PACK (50268-605-11) | 50 blister pack | 2017-03-14 | 0000-00-00 | No | No | Current |