United States · FDA National Drug Code directory
Amitriptyline Hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 50090-7424_cfbea0b3-d501-4285-a38f-4ea27877f77b
- Product NDC
- 50090-7424
- Form
- TABLET, COATED
- Composition / generic term
- Amitriptyline Hydrochloride
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240520
- Source listing expiry
- 20271231
Source-listed ingredients
- AMITRIPTYLINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, COATED in 1 BOTTLE (50090-7424-0) · 50090-7424-0
- 100 TABLET, COATED in 1 BOTTLE (50090-7424-1) · 50090-7424-1
- 90 TABLET, COATED in 1 BOTTLE (50090-7424-6) · 50090-7424-6
- 60 TABLET, COATED in 1 BOTTLE (50090-7424-7) · 50090-7424-7
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →