Nortriptyline Hydrochloride
- Product NDC
- 50436-6651
- 11-digit product format
- 504366651
- Labeler code
- 50436
- Product ID
- 50436-6651_984f18b4-55ac-42b1-abe8-37f2a2147dad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA073555
- Marketing category
- ANDA
- Marketing start
- 1992-07-01
- 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
- 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 | 50436-6651 | D | Discontinued by firm | 2026-08-03 | ||
| excluded package | package | 50436-6651 | 50436-6651-2 | D | Discontinued by firm | 2026-08-03 | |
| excluded package | package | 50436-6651 | 50436-6651-3 | D | Discontinued by firm | 2026-08-03 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50436-6651-2 | EA - Each | 50436-6651 | b741b2c4-a5cd-4eda-bf84-810e2303bdf7 | 1 | 2014-12-01 |