Nortriptyline Hydrochloride
- Product NDC
- 35356-651
- 11-digit product format
- 353560651
- Labeler code
- 35356
- Product ID
- 35356-651_eb834045-6333-4d82-9b2a-1d221d1d89c0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA073553
- Marketing category
- ANDA
- Marketing start
- 1992-07-01
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 35356-651 | D | Discontinued by firm | 2026-08-03 | ||
| excluded package | package | 35356-651 | 35356-651-30 | D | Discontinued by firm | 2026-08-03 | |
| excluded package | package | 35356-651 | 35356-651-60 | D | Discontinued by firm | 2026-08-03 | |
| excluded package | package | 35356-651 | 35356-651-90 | D | Discontinued by firm | 2026-08-03 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 35356-651-30 | EA - Each | 35356-651 | 33dbbb08-e3ab-44f3-a63d-9a2f63720fe6 | 1 | 2013-06-04 |
| 35356-651-60 | EA - Each | 35356-651 | 75322720-7566-4a6c-8035-eb25b3f512db | 1 | 2013-06-04 |