NDC 71335-0200 – Clindamycin hydrochloride

Clindamycin Hydrochloride 150 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-0200

Product details

Brand name
Clindamycin hydrochloride
Generic name
Clindamycin hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA065061
Marketed since
March 23, 2001
Listing expires
December 31, 2026
Pharmacologic class
Lincosamide Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Clindamycin Hydrochloride →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0200-040 CAPSULE in 1 BOTTLE (71335-0200-0)Feb 26, 2018
71335-0200-112 CAPSULE in 1 BOTTLE (71335-0200-1)Apr 22, 2019
71335-0200-228 CAPSULE in 1 BOTTLE (71335-0200-2)Feb 13, 2018
71335-0200-342 CAPSULE in 1 BOTTLE (71335-0200-3)Oct 16, 2018
71335-0200-460 CAPSULE in 1 BOTTLE (71335-0200-4)Mar 2, 2018
71335-0200-530 CAPSULE in 1 BOTTLE (71335-0200-5)Mar 20, 2018
71335-0200-621 CAPSULE in 1 BOTTLE (71335-0200-6)Apr 2, 2019
71335-0200-74 CAPSULE in 1 BOTTLE (71335-0200-7)Sep 5, 2024
71335-0200-856 CAPSULE in 1 BOTTLE (71335-0200-8)Sep 5, 2024
71335-0200-920 CAPSULE in 1 BOTTLE (71335-0200-9)Mar 23, 2018

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