0615-6581 : Simvastatin 40 mg Oral Tablet

NDC:	0615-6581
Labeler:	Ncs Healthcare of Ky, Inc Dba Vangard Labs
Product Type:	Human Prescription Drug
Drug Name:	Simvastatin
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA077752
Rev. Date:	Dec 20, 2006

Appearance:

Markings:	RDY;200
Shapes:	Round
Colors:	Brown
Size (mm):	10
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.

NDC Package Codes:

0615-6581-39: 30 TABLET, FILM COATED IN 1 BLISTER PACK (0615‑6581‑39)

Active Ingredients:

Simvastatin

Dosage Strength:

40 mg

Inactive Ingredients:

Ascorbic Acid
Butylated Hydroxyanisole
Anhydrous Citric Acid
Hydroxypropyl Cellulose
Hypromelloses
Ferrosoferric Oxide
Ferric Oxide Red
Ferric Oxide Yellow
Isopropyl Alcohol
Lactose Monohydrate
Magnesium Stearate
Cellulose, Microcrystalline
Starch, Corn
Titanium Dioxide

Pharmaceutical Classes:

HMG-CoA Reductase Inhibitor [EPC]
Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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.