NDC 64380-713 – Benzonatate

Benzonatate 200 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC64380-713

Product details

Brand name
Benzonatate
Generic name
Benzonatate
Labeler
Strides Pharma Science Limited
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA091133
Marketed since
May 29, 2026
Listing expires
December 31, 2027
Pharmacologic class
Non-narcotic Antitussive

Active ingredients

Uses, dosage, side effects and warnings for Benzonatate →

Package NDC codes (2)

Package NDCDescriptionSince
64380-713-06100 CAPSULE in 1 CONTAINER (64380-713-06)May 29, 2026
64380-713-07500 CAPSULE in 1 BOTTLE (64380-713-07)May 29, 2026

Recalls mentioning this NDC

Other Benzonatate products