NDC 82804-980 – Famotidine

Famotidine 20 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC82804-980

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Proficient Rx LP
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA217669
Marketed since
September 9, 2024
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (9)

Package NDCDescriptionSince
82804-980-00100 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-980-00)Jan 27, 2025
82804-980-2020 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-980-20)Jan 27, 2025
82804-980-3030 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-980-30)Jan 27, 2025
82804-980-55500 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-980-55)Jan 27, 2025
82804-980-6060 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-980-60)Jan 27, 2025
82804-980-67270 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-980-67)Jan 27, 2025
82804-980-72120 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-980-72)Jan 27, 2025
82804-980-78180 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-980-78)Jan 27, 2025
82804-980-9090 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-980-90)Jan 27, 2025

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