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
- 60760-732_485b7f90-31f1-0f8d-e063-6294a90a4866
- Product NDC
- 60760-732
- Form
- TABLET
- Composition / generic term
- Amitriptyline Hydrochloride
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230610
- Source listing expiry
- 20271231
Source-listed ingredients
- AMITRIPTYLINE HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET in 1 BOTTLE, PLASTIC (60760-732-90) · 60760-732-90
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 →