United States · FDA National Drug Code directory
Tramadol 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
- 70518-3824_5449e98d-a7b8-2bee-e063-6394a90a111f
- Product NDC
- 70518-3824
- Form
- TABLET, COATED
- Composition / generic term
- Tramadol Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230807
- Source listing expiry
- 20271231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, COATED in 1 BLISTER PACK (70518-3824-0) · 70518-3824-0
- 60 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-1) · 70518-3824-1
- 90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-2) · 70518-3824-2
- 180 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-3) · 70518-3824-3
- 120 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-4) · 70518-3824-4
- 30 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-5) · 70518-3824-5
- 100 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-6) · 70518-3824-6
- 180 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-7) · 70518-3824-7
- 90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-8) · 70518-3824-8
- 180 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-9) · 70518-3824-9
Source and coverage
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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.
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