NDC 69097-168 – Arformoterol tartrate

Arformoterol Tartrate 15 ug/2mL · Solution · Respiratory (inhalation)

Human Prescription Drug 1 recall

Product NDC69097-168

Product details

Brand name
Arformoterol tartrate
Generic name
Arformoterol tartrate
Labeler
Cipla USA Inc.
Dosage form
Solution
Route
Respiratory (inhalation)
Marketing category
ANDA · ANDA207306
Marketed since
June 22, 2021
Listing expires
December 31, 2026
Pharmacologic class
beta2-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Arformoterol Tartrate →

Package NDC codes (3)

Package NDCDescriptionSince
69097-168-5330 POUCH in 1 CARTON (69097-168-53) / 1 VIAL, SINGLE-DOSE in 1 POUCH (69097-168-32) / 2 mL in 1 VIAL, SINGLE-DOSEJan 27, 2022
69097-168-6412 POUCH in 1 CARTON (69097-168-64) / 5 VIAL, SINGLE-DOSE in 1 POUCH / 2 mL in 1 VIAL, SINGLE-DOSEJun 22, 2021
69097-168-876 POUCH in 1 CARTON (69097-168-87) / 5 VIAL, SINGLE-DOSE in 1 POUCH (69097-168-48) / 2 mL in 1 VIAL, SINGLE-DOSEJun 22, 2021

Recalls mentioning this NDC

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