NDC 71335-2141 – Tetracycline Hydrochloride

Tetracycline Hydrochloride 500 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2141

Product details

Brand name
Tetracycline Hydrochloride
Generic name
Tetracycline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA210662
Marketed since
January 18, 2019
Listing expires
December 31, 2026
Pharmacologic class
Tetracycline-class Antimicrobial

Active ingredients

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

Package NDC codes (8)

Package NDCDescriptionSince
71335-2141-160 CAPSULE in 1 BOTTLE, PLASTIC (71335-2141-1)Apr 3, 2024
71335-2141-240 CAPSULE in 1 BOTTLE, PLASTIC (71335-2141-2)Apr 3, 2024
71335-2141-330 CAPSULE in 1 BOTTLE, PLASTIC (71335-2141-3)Jul 29, 2022
71335-2141-456 CAPSULE in 1 BOTTLE, PLASTIC (71335-2141-4)Apr 3, 2024
71335-2141-528 CAPSULE in 1 BOTTLE, PLASTIC (71335-2141-5)Apr 3, 2024
71335-2141-620 CAPSULE in 1 BOTTLE, PLASTIC (71335-2141-6)Apr 3, 2024
71335-2141-790 CAPSULE in 1 BOTTLE, PLASTIC (71335-2141-7)Apr 3, 2024
71335-2141-845 CAPSULE in 1 BOTTLE, PLASTIC (71335-2141-8)Apr 3, 2024

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