NDC 82644-870 – Tetracycline Hydrochloride

Tetracycline Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC82644-870

Product details

Brand name
Tetracycline Hydrochloride
Generic name
Tetracycline Hydrochloride
Labeler
Pharmaka Generics Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA061147
Marketed since
January 19, 2024
Listing expires
December 31, 2026
Pharmacologic class
Tetracycline-class Antimicrobial

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
82644-870-6060 TABLET, FILM COATED in 1 BOTTLE (82644-870-60)Jan 19, 2024

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