United States · FDA National Drug Code directory
Lidocaine 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
- 17856-0138_34f4d3da-f769-0bdd-e063-6394a90a3fa1
- Product NDC
- 17856-0138
- Form
- SOLUTION
- Composition / generic term
- Lidocaine hydrochloride
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230328
- Source listing expiry
- 20261231
Source-listed ingredients
- LIDOCAINE HYDROCHLORIDE — 20 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0138-1) / 15 mL in 1 CUP, UNIT-DOSE (17856-0138-3) · 17856-0138-1
- 50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0138-2) / 20 mL in 1 CUP, UNIT-DOSE (17856-0138-4) · 17856-0138-2
- 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0138-5) / 5 mL in 1 CUP, UNIT-DOSE (17856-0138-6) · 17856-0138-5
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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