Nortriptyline Hydrochloride
- Product NDC
- 55700-668
- 11-digit product format
- 557000668
- Labeler code
- 55700
- Product ID
- 55700-668_1853f9fb-b2b5-4c1e-9888-f3591afb0bff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA075520
- Marketing category
- ANDA
- Marketing start
- 2018-08-17
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55700-668 | NORTRIPTYLINE HYDROCHLORIDE CAPSULE [QUALITY CARE PRODUCTS LLC] | 7 | Legacy NDC | 20241220_4f907f4e-9aab-4d9d-bd24-8d55fe4817a2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-668-30 | 55700066830 | 30 CAPSULE in 1 BOTTLE (55700-668-30) | 30 capsule | 2018-08-17 | 0000-00-00 | No | No | Current |
| 55700-668-60 | 55700066860 | 60 CAPSULE in 1 BOTTLE (55700-668-60) | 60 capsule | 2020-03-20 | 0000-00-00 | No | No | Current |