72162-1733 : Diclofenac Sodium Delayed Release 50 mg Oral Tablet, Delayed Release

NDC:	72162-1733
Labeler:	Bryant Ranch Prepack
Product Type:	Human Prescription Drug
Drug Name:	Diclofenac Sodium Delayed Release
Dosage Form:	Oral Tablet, Delayed Release
Application #:	ANDA075185
Rev. Date:	Nov 13, 1998

NDC Package Codes:

72162-1733-0: 1000 TABLET, DELAYED RELEASE IN 1 BOTTLE, PLASTIC (72162‑1733‑0)
72162-1733-1: 100 TABLET, DELAYED RELEASE IN 1 BOTTLE, PLASTIC (72162‑1733‑1)
72162-1733-2: 120 TABLET, DELAYED RELEASE IN 1 BOTTLE, PLASTIC (72162‑1733‑2)
72162-1733-3: 30 TABLET, DELAYED RELEASE IN 1 BOTTLE, PLASTIC (72162‑1733‑3)
72162-1733-6: 60 TABLET, DELAYED RELEASE IN 1 BOTTLE, PLASTIC (72162‑1733‑6)
72162-1733-7: 14 TABLET, DELAYED RELEASE IN 1 BOTTLE, PLASTIC (72162‑1733‑7)
72162-1733-8: 1000 TABLET, DELAYED RELEASE IN 1 BOTTLE, PLASTIC (72162‑1733‑8)
72162-1733-9: 90 TABLET, DELAYED RELEASE IN 1 BOTTLE, PLASTIC (72162‑1733‑9)

Active Ingredients:

Diclofenac Sodium

Dosage Strength:

50 mg

Pharmaceutical Classes:

Anti-Inflammatory Agents
Non-Steroidal [CS]
Cyclooxygenase Inhibitors [MoA]
Decreased Prostaglandin Production [PE]
Nonsteroidal Anti-inflammatory Drug [EPC]

NDC QR Code

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NDC 72162-1733 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.