50090-1317 : Etodolac 600 mg Oral Tablet, Film Coated, Extended Release

NDC:	50090-1317
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Etodolac
Dosage Form:	Oral Tablet, Film Coated, Extended Release
Application #:	ANDA091134
Rev. Date:	Feb 15, 2014

Appearance:

Markings:	273
Shapes:	Oval
Colors:	Blue
Size (mm):	19
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:

50090-1317-0: 15 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (50090‑1317‑0)
50090-1317-1: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (50090‑1317‑1)

Active Ingredients:

Etodolac

Dosage Strength:

600 mg

Inactive Ingredients:

Sodium Phosphate, Dibasic, Anhydrous
Ethylcellulose (100 Mpa.s)
Fd&c Blue No. 2
Ferric Oxide Red
Ferric Oxide Yellow
Hypromellose, Unspecified
Lactose Monohydrate
Magnesium Stearate
Polyethylene Glycol, Unspecified
Talc
Titanium Dioxide
Triacetin

Pharmaceutical Classes:

Cyclooxygenase Inhibitors [MoA]
Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient]
Nonsteroidal Anti-inflammatory Drug [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.