NDC 51662-1619 – Atropine Sulfate

Atropine Sulfate .4 mg/mL · Injection · Endotracheal, Intramedullary, Intramuscular, Intravenous, Subcutaneous

Human Prescription Drug

Product NDC51662-1619

Product details

Brand name
Atropine Sulfate
Generic name
Atropine Sulfate
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Dosage form
Injection
Route
Endotracheal, Intramedullary, Intramuscular, Intravenous, Subcutaneous
Marketing category
ANDA · ANDA213561
Marketed since
October 1, 2022
Listing expires
December 31, 2026
Pharmacologic class
Anticholinergic; Cholinergic Muscarinic Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Atropine sulfate →

Package NDC codes (2)

Package NDCDescriptionSince
51662-1619-120 mL in 1 VIAL (51662-1619-1)Nov 10, 2022
51662-1619-310 POUCH in 1 CASE (51662-1619-3) / 1 VIAL in 1 POUCH (51662-1619-2) / 20 mL in 1 VIALOct 1, 2022

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