Amitriptyline Hydrochloride
- Product NDC
- 49999-228
- 11-digit product format
- 499990228
- Labeler code
- 49999
- Product ID
- 49999-228_fb2f3471-0169-4eaa-9a11-c32129ba651b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amitriptyline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA040218
- Marketing category
- ANDA
- Marketing start
- 2010-09-01
- Marketing end
- 0000-00-00
- Substance
- AMITRIPTYLINE 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