55154-5369 : Ondansetron 4 mg (Ondansetron Hydrochloride Dihydrate 5 mg) Oral Tablet

NDC:	55154-5369
Labeler:	Cardinal Health
Product Type:	Human Prescription Drug
Drug Name:	Ondansetron
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA076930
Rev. Date:	Dec 5, 2012

Appearance:

Markings:	M;315
Shapes:	Round
Colors:	White
Size (mm):	6
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.

M 315: (0378-0315) Ondansetron 4 mg (Ondansetron Hydrochloride Dihydrate 5 mg) Oral Tablet by Cardinal Health

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:

55154-5369-0: 1 BLISTER PACK IN 1 BAG (55154‑5369‑0) > 10 TABLET, FILM COATED IN 1 BLISTER PACK

Active Ingredients:

Ondansetron Hydrochloride

Dosage Strength:

4 mg

Inactive Ingredients:

Anhydrous Lactose
Silicon Dioxide
Croscarmellose Sodium
Hypromelloses
Magnesium Stearate
Cellulose, Microcrystalline
Polydextrose
Polyethylene Glycols
Starch, Corn
Sodium Lauryl Sulfate
Titanium Dioxide
Triacetin

Pharmaceutical Classes:

Serotonin 3 Receptor Antagonists [MoA]
Serotonin-3 Receptor Antagonist [EPC]

NDC 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.