55289-014 : Lunesta 3 mg Oral Tablet

NDC:	55289-014
Labeler:	Pd-rx Pharmaceuticals, Inc.
Product Type:	Human Prescription Drug
Drug Name:	Lunesta
Dosage Form:	Oral Tablet, Coated
Application #:	NDA021476
Rev. Date:	Apr 4, 2005
CSA Schedule:	CIV (US) ^[1]

^[1] Schedule IV Controlled Substance: Low potential for abuse relative to substances in Schedule III. Examples include Alprazolam (Xanax), Diazepam (Valium), Carisoprodol (Soma), Clonazepam (Klonopin), Lorazepam (Ativan), Clorazepate (Tranxene), Midazolam (Versed), Temazepam (Restoril), and Triazolam (Halcion).. More Details: US Dept of Justice Controlled Substance Schedules.

Appearance:

Markings:	S193
Shapes:	Round
Colors:	Blue
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.

S193: (63402-193) Lunesta 3 mg Oral Tablet by Pd-rx Pharmaceuticals, Inc.

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:

55289-014-30: 30 TABLET, COATED IN 1 BOTTLE, PLASTIC (55289‑014‑30)

Active Ingredients:

Eszopiclone

Dosage Strength:

3 mg

Inactive Ingredients:

Anhydrous Dibasic Calcium Phosphate
Silicon Dioxide
Croscarmellose Sodium
Hypromellose 2910 (6 Mpa.s)
Lactose Monohydrate
Magnesium Stearate
Cellulose, Microcrystalline
Polyethylene Glycol
Titanium Dioxide
Triacetin
Fd&c Blue No. 2

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.