United States · FDA National Drug Code directory
Meperidine 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
- 42806-050_a2109eab-1e10-4549-adee-0700efae6f3c
- Product NDC
- 42806-050
- Form
- TABLET
- Composition / generic term
- Meperidine Hydrochloride
- Labeler
- EPIC PHARMA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110505
- Source listing expiry
- 20261231
Source-listed ingredients
- MEPERIDINE HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (42806-050-01) · 42806-050-01
- 30 TABLET in 1 BOTTLE (42806-050-30) · 42806-050-30
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 →