United States · FDA National Drug Code directory
PHENYLEPHRINE 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
- 70069-802_90a3853e-49d6-4536-be72-82cc875bcf74
- Product NDC
- 70069-802
- Form
- INJECTION
- Composition / generic term
- PHENYLEPHRINE HYDROCHLORIDE
- Labeler
- Somerset Therapeutics, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210922
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENYLEPHRINE HYDROCHLORIDE — 50 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (70069-802-10) / 5 mL in 1 VIAL, PHARMACY BULK PACKAGE (70069-802-01) · 70069-802-10
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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