35356-725 : Diclofenac Sodium 50 mg Delayed Release Tablet

NDC:	35356-725
Labeler:	Lake Erie Medical Dba Quality Care Products LLC
Product Type:	Human Prescription Drug
Drug Name:	Diclofenac Sodium
Dosage Form:	Oral Tablet, Delayed Release
Application #:	ANDA090066
Rev. Date:	Dec 31, 2010

Appearance:

Markings:	P;50
Shapes:	Round
Colors:	Brown
Size (mm):	8
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.

P 50: (16571-202) Diclofenac Sodium 50 mg Delayed Release Tablet by Lake Erie Medical Dba Quality Care Products LLC

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:

35356-725-30: 30 TABLET, DELAYED RELEASE IN 1 BOTTLE (35356‑725‑30)
35356-725-60: 60 TABLET, DELAYED RELEASE IN 1 BOTTLE (35356‑725‑60)
35356-725-90: 90 TABLET, DELAYED RELEASE IN 1 BOTTLE (35356‑725‑90)

Active Ingredients:

Diclofenac Sodium

Dosage Strength:

50 mg

Inactive Ingredients:

Lactose Monohydrate
Cellulose, Microcrystalline
Croscarmellose Sodium
Povidone
Talc
Magnesium Stearate
Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
Polyethylene Glycols
Titanium Dioxide
Hypromelloses
Ferric Oxide Red
Ferric Oxide Yellow
Water

Pharmaceutical Classes:

Cyclooxygenase Inhibitors [MoA]
Decreased Prostaglandin Production [PE]
Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient]
Nonsteroidal Anti-inflammatory Drug [EPC]

NDC QR Code

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NDC 35356-725 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.