NDC 71335-3170 – Tetracycline Hydrochloride

Tetracycline Hydrochloride 250 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-3170

Product details

Brand name
Tetracycline Hydrochloride
Generic name
Tetracycline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA062752
Marketed since
April 1, 2020
Listing expires
December 31, 2027
Pharmacologic class
Tetracycline-class Antimicrobial

Active ingredients

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

Package NDC codes (8)

Package NDCDescriptionSince
71335-3170-120 CAPSULE in 1 BOTTLE (71335-3170-1)Aug 11, 2026
71335-3170-240 CAPSULE in 1 BOTTLE (71335-3170-2)Aug 11, 2026
71335-3170-360 CAPSULE in 1 BOTTLE (71335-3170-3)Aug 11, 2026
71335-3170-430 CAPSULE in 1 BOTTLE (71335-3170-4)Aug 11, 2026
71335-3170-528 CAPSULE in 1 BOTTLE (71335-3170-5)Aug 11, 2026
71335-3170-6112 CAPSULE in 1 BOTTLE (71335-3170-6)Aug 11, 2026
71335-3170-76 CAPSULE in 1 BOTTLE (71335-3170-7)Aug 11, 2026
71335-3170-810 CAPSULE in 1 BOTTLE (71335-3170-8)Aug 11, 2026

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