United States · FDA National Drug Code directory
Duloxetine
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
- 70518-1244_58b4ec4f-c6d3-ce06-e063-6394a90a3a05
- Product NDC
- 70518-1244
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Duloxetine
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180605
- Source listing expiry
- 20271231
Source-listed ingredients
- DULOXETINE HYDROCHLORIDE — 60 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1244-0) · 70518-1244-0
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1244-1) · 70518-1244-1
- 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1244-3) · 70518-1244-3
- 50 POUCH in 1 BOX (70518-1244-4) / 1 CAPSULE, DELAYED RELEASE in 1 POUCH (70518-1244-5) · 70518-1244-4
- 50 POUCH in 1 BOX (70518-1244-6) / 1 CAPSULE, DELAYED RELEASE in 1 POUCH (70518-1244-7) · 70518-1244-6
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1244-8) · 70518-1244-8
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1244-9) · 70518-1244-9
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 →