Amitriptyline Hydrochloride
- Product NDC
- 35356-742
- 11-digit product format
- 353560742
- Labeler code
- 35356
- Product ID
- 35356-742_54da0e4c-8478-498b-b100-fc09b2719c26
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amitriptyline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
- Application
- ANDA085968
- Marketing category
- ANDA
- Marketing start
- 1977-11-29
- 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