0093-0739 : Donepezil Hydrochloride 10 mg Oral Tablet

NDC:	0093-0739
Labeler:	Teva Pharmaceuticals USA Inc
Product Type:	Human Prescription Drug
Drug Name:	Donepezil Hydrochloride
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA090425
Rev. Date:	May 31, 2011

Appearance:

Markings:	TEVA;739
Shapes:	Round
Colors:	Yellow
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 739: (0093-0739) Donepezil Hydrochloride 10 mg Oral Tablet by Teva Pharmaceuticals USA 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:

0093-0739-05: 500 TABLET, FILM COATED IN 1 BOTTLE (0093‑0739‑05)
0093-0739-56: 30 TABLET, FILM COATED IN 1 BOTTLE (0093‑0739‑56)
0093-0739-98: 90 TABLET, FILM COATED IN 1 BOTTLE (0093‑0739‑98)

Active Ingredients:

Donepezil Hydrochloride

Dosage Strength:

10 mg

Inactive Ingredients:

Silicon Dioxide
Starch, Corn
Hypromelloses
Lactose Monohydrate
Magnesium Stearate
Cellulose, Microcrystalline
Polyethylene Glycols
Sodium Starch Glycolate Type a Potato
Titanium Dioxide
Ferric Oxide Yellow

Pharmaceutical Classes:

Cholinesterase Inhibitor [EPC]
Cholinesterase Inhibitors [MoA]

NDC QR Code

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NDC 0093-0739 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.