United States · FDA National Drug Code directory
Naropin
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
- 63323-288_cdcd6c58-85cf-4d7e-9d97-b7c282a4f6b9
- Product NDC
- 63323-288
- Form
- INJECTION, SOLUTION
- Composition / generic term
- ROPIVACAINE HYDROCHLORIDE
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 19960924
- Source listing expiry
- 20261231
Source-listed ingredients
- ROPIVACAINE HYDROCHLORIDE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 5 AMPULE in 1 BOX (63323-288-10) / 10 mL in 1 AMPULE (63323-288-01) · 63323-288-10
- 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-288-11) / 10 mL in 1 VIAL, SINGLE-DOSE (63323-288-03) · 63323-288-11
- 5 AMPULE in 1 BOX (63323-288-20) / 20 mL in 1 AMPULE (63323-288-06) · 63323-288-20
- 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-288-21) / 20 mL in 1 VIAL, SINGLE-DOSE (63323-288-07) · 63323-288-21
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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