Nortriptyline Hydrochloride
- Product NDC
- 60687-281
- 11-digit product format
- 606870281
- Labeler code
- 60687
- Product ID
- 60687-281_d659b0c7-e4d7-265f-e053-2a95a90adfc0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA075520
- Marketing category
- ANDA
- Marketing start
- 2017-06-02
- 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 |
|---|
| 60687-281 | NORTRIPTYLINE HYDROCHLORIDE CAPSULE [AMERICAN HEALTH PACKAGING] | 8 | Legacy NDC | 20240809_a4bdbe16-79f8-486f-8ac5-4fa8bf4131e5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-281-01 | 60687028101 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-281-01) > 1 CAPSULE in 1 BLISTER PACK (60687-281-11) | 100 blister pack | 2017-06-02 | 0000-00-00 | No | No | Current |