Amitriptyline Hydrochloride
- Product NDC
- 51079-133
- 11-digit product format
- 510790133
- Labeler code
- 51079
- Product ID
- 51079-133_b4dca9ec-6443-a7e7-e053-2a95a90ad720
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- amitriptyline hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA086009
- Marketing category
- ANDA
- Marketing start
- 1994-10-26
- Marketing end
- 2021-01-31
- Substance
- AMITRIPTYLINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Tricyclic Antidepressant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record