Amitriptyline Hydrochloride
- Product NDC
- 50090-0030
- 11-digit product format
- 500900030
- Labeler code
- 50090
- Product ID
- 50090-0030_65b0e128-fcf7-4de7-ba34-1cb9367e0d55
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amitriptyline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040218
- Marketing category
- ANDA
- Marketing start
- 1997-09-11
- Marketing end
- 0000-00-00
- Substance
- AMITRIPTYLINE H
- Active strength
- 10 mg/1
- Pharmacologic classes
- Tricyclic Antid
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record