NDC 68382-623 – Buspirone hydrochloride

Buspirone Hydrochloride 7.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68382-623

Product details

Brand name
Buspirone hydrochloride
Generic name
Buspirone hydrochloride
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078888
Marketed since
March 21, 2023
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Buspirone hydrochloride →

Package NDC codes (4)

Package NDCDescriptionSince
68382-623-01100 TABLET in 1 BOTTLE (68382-623-01)Mar 21, 2023
68382-623-05500 TABLET in 1 BOTTLE (68382-623-05)Mar 21, 2023
68382-623-101000 TABLET in 1 BOTTLE (68382-623-10)Mar 21, 2023
68382-623-30100 BLISTER PACK in 1 CARTON (68382-623-30) / 10 TABLET in 1 BLISTER PACKMar 21, 2023

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