NDC 68084-214 – Benzonatate

Benzonatate 100 mg/1 · Capsule · Oral

Human Prescription Drug 2 recalls

Product NDC68084-214

Product details

Brand name
Benzonatate
Generic name
Benzonatate
Labeler
American Health Packaging
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA040597
Marketed since
May 26, 2021
Listing expires
December 31, 2026
Pharmacologic class
Non-narcotic Antitussive

Active ingredients

Uses, dosage, side effects and warnings for Benzonatate →

Package NDC codes (1)

Package NDCDescriptionSince
68084-214-0110 BLISTER PACK in 1 CARTON (68084-214-01) / 10 CAPSULE in 1 BLISTER PACK (68084-214-11)May 26, 2021

Recalls mentioning this NDC

Other Benzonatate products