47335-816 : Atomoxetine 25 mg (As Atomoxetine Hydrochloride) Oral Capsule

NDC:	47335-816
Labeler:	Sun Pharma Global Fze
Product Type:	Human Prescription Drug
Drug Name:	Atomoxetine Hydrochloride
Dosage Form:	Oral Capsule
Application #:	ANDA079020
Rev. Date:	Oct 5, 2010

Appearance:

Markings:	816
Shapes:	Capsule
Colors:	Blue / White
Size (mm):	16
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:

47335-816-08: 100 CAPSULE IN 1 BOTTLE (47335‑816‑08)
47335-816-18: 1000 CAPSULE IN 1 BOTTLE (47335‑816‑18)
47335-816-83: 30 CAPSULE IN 1 BOTTLE (47335‑816‑83)
47335-816-88: 100 CAPSULE IN 1 BOTTLE (47335‑816‑88)

Active Ingredients:

Atomoxetine Hydrochloride

Dosage Strength:

25 mg

Inactive Ingredients:

Starch, Corn
Silicon Dioxide
Gelatin
Sodium Lauryl Sulfate
Titanium Dioxide
Fd&c Blue No. 2

Pharmaceutical Classes:

Norepinephrine Reuptake Inhibitor [EPC]
Norepinephrine Uptake 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.