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