United States · FDA National Drug Code directory
vasopressin
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
- 70121-1642_852dfca1-d3f4-4c85-8140-1b74e464ec0c
- Product NDC
- 70121-1642
- Form
- INJECTION
- Composition / generic term
- vasopressin
- Labeler
- Amneal Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220811
- Source listing expiry
- 20261231
Source-listed ingredients
- VASOPRESSIN — 20 [USP'U]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 CARTON (70121-1642-2) / 1 mL in 1 VIAL (70121-1642-1) · 70121-1642-2
- 25 VIAL in 1 CARTON (70121-1642-5) / 1 mL in 1 VIAL (70121-1642-1) · 70121-1642-5
- 10 VIAL in 1 CARTON (70121-1642-7) / 1 mL in 1 VIAL (70121-1642-1) · 70121-1642-7
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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