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
- 71335-3007_38ed32d4-0f8d-491c-8c67-7b38d7d72513
- Product NDC
- 71335-3007
- Form
- TABLET, COATED
- Composition / generic term
- Amitriptyline Hydrochloride
- Labeler
- Bryant Ranch Prepack
- 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
- 100 TABLET, COATED in 1 BOTTLE (71335-3007-0) · 71335-3007-0
- 30 TABLET, COATED in 1 BOTTLE (71335-3007-1) · 71335-3007-1
- 15 TABLET, COATED in 1 BOTTLE (71335-3007-2) · 71335-3007-2
- 60 TABLET, COATED in 1 BOTTLE (71335-3007-3) · 71335-3007-3
- 90 TABLET, COATED in 1 BOTTLE (71335-3007-4) · 71335-3007-4
- 28 TABLET, COATED in 1 BOTTLE (71335-3007-5) · 71335-3007-5
- 120 TABLET, COATED in 1 BOTTLE (71335-3007-6) · 71335-3007-6
- 50 TABLET, COATED in 1 BOTTLE (71335-3007-7) · 71335-3007-7
- 180 TABLET, COATED in 1 BOTTLE (71335-3007-8) · 71335-3007-8
- 6 TABLET, COATED in 1 BOTTLE (71335-3007-9) · 71335-3007-9
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 →