NDC 82804-981 – Famotidine

Famotidine 40 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC82804-981

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
82804-981-00100 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-981-00)Jan 27, 2025
82804-981-2020 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-981-20)Jan 27, 2025
82804-981-3030 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-981-30)Jan 27, 2025
82804-981-55500 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-981-55)Jan 27, 2025
82804-981-6060 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-981-60)Jan 27, 2025
82804-981-67270 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-981-67)Jan 27, 2025
82804-981-72120 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-981-72)Jan 27, 2025
82804-981-78180 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-981-78)Jan 27, 2025
82804-981-9090 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-981-90)Jan 27, 2025

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