NDC 42708-082 – Benzonatate

Benzonatate 200 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC42708-082

Product details

Brand name
Benzonatate
Generic name
Benzonatate
Labeler
QPharma, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA040627
Marketed since
March 22, 2017
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
42708-082-21 sample21 CAPSULE in 1 BOTTLE (42708-082-21)Feb 28, 2019

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