United States · FDA National Drug Code directory

Diluent

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
61434-011_3c4350ea-c3f8-12ad-e063-6394a90a6402
Product NDC
61434-011
Form
SOLUTION
Composition / generic term
Diluent
Labeler
Catalent Indiana, LLC
Marketing category
DRUG FOR FURTHER PROCESSING
Marketing start / end (source format)
20171006 / 20280331

Source-listed ingredients

  • CARBOXYMETHYLCELLULOSE SODIUM — 25 mg/5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 5 mL in 1 VIAL (61434-011-00) · 61434-011-00

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.

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