Nortriptyline Hydrochloride
- Product NDC
- 0179-0223
- 11-digit product format
- 001790223
- Labeler code
- 0179
- Product ID
- 0179-0223_7b34fae3-1ad3-4c8f-e053-2a91aa0a3430
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nortriptyline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- KAISER FOUNDATION HOSPITA
- Application
- ANDA073553
- Marketing category
- ANDA
- Marketing start
- 2017-01-17
- Marketing end
- 2019-03-31
- Substance
- NORTRIPTYLINE H
- Active strength
- 10 mg/1
- Pharmacologic classes
- Tricyclic Antid
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 | 0179-0223 | D | Discontinued by firm | 2026-08-03 | ||
| excluded package | package | 0179-0223 | 0179-0223-15 | D | Discontinued by firm | 2026-08-03 |