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: 70069-813_18b65b44-fdd1-4385-b6f8-cf3cbdc8d0e6
Product NDC: 70069-813
Form: INJECTION
Composition / generic term: PHENYLEPHRINE HYDROCHLORIDE
Labeler: Somerset Therapeutics, LLC
Marketing category: ANDA
Marketing start / end (source format): 20230717
Source listing expiry: 20261231

Source-listed ingredients

PHENYLEPHRINE HYDROCHLORIDE — 100 mg/10mL

These values do not establish equivalence or a dose recommendation.

Packages

1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (70069-813-01) / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE · 70069-813-01

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.

Browse United States records →