50090-1044 : Famotidine 20 mg Oral Tablet, Film Coated

NDC:	50090-1044
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Famotidine
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA075511
Rev. Date:	Apr 16, 2001

Appearance:

Markings:	TEVA;5728
Shapes:	Round
Colors:	Brown
Size (mm):	9
Segments: ^*	1
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

TEVA 5728: (0172-5728) Famotidine 20 mg Oral Tablet, Film Coated by A-s Medication Solutions

The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

50090-1044-0: 30 TABLET, FILM COATED IN 1 BOTTLE (50090‑1044‑0)
50090-1044-1: 20 TABLET, FILM COATED IN 1 BOTTLE (50090‑1044‑1)
50090-1044-2: 60 TABLET, FILM COATED IN 1 BOTTLE (50090‑1044‑2)
50090-1044-3: 90 TABLET, FILM COATED IN 1 BOTTLE (50090‑1044‑3)

Active Ingredients:

Famotidine

Dosage Strength:

20 mg

Inactive Ingredients:

Silicon Dioxide
Hypromellose, Unspecified
Magnesium Stearate
Microcrystalline Cellulose
Polyethylene Glycol 3000
Polyethylene Glycol 4000
Starch, Corn
Sodium Starch Glycolate Type a Potato
Talc
Titanium Dioxide
Ferric Oxide Yellow
Lactose Monohydrate
Ferric Oxide Red
Triacetin /

Pharmaceutical Classes:

Histamine H2 Receptor Antagonists [MoA]
Histamine-2 Receptor Antagonist [EPC]

NDC QR Code

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NDC 50090-1044 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.