United States · FDA National Drug Code directory
DULOXETINE DELAYED-RELEASE
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
- 63187-702_baacd94b-8cee-45ad-9bb4-cd12a8cfbd58
- Product NDC
- 63187-702
- Form
- CAPSULE, DELAYED RELEASE PELLETS
- Composition / generic term
- DULOXETINE HYDROCHLORIDE
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140611
- Source listing expiry
- 20261231
Source-listed ingredients
- DULOXETINE HYDROCHLORIDE — 30 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-30) · 63187-702-30
- 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-60) · 63187-702-60
- 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-90) · 63187-702-90
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 →