United States · FDA National Drug Code directory
Verapamil 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
- 70069-272_8eb0d81b-28fc-41a7-bf53-3d4217a740f2
- Product NDC
- 70069-272
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Verapamil Hydrochloride
- Labeler
- Somerset Therapeutics, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180618
- Source listing expiry
- 20271231
Source-listed ingredients
- VERAPAMIL HYDROCHLORIDE — 2.5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 5 VIAL in 1 CARTON (70069-272-05) / 4 mL in 1 VIAL · 70069-272-05
- 25 VIAL in 1 CARTON (70069-272-25) / 4 mL in 1 VIAL (70069-272-01) · 70069-272-25
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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