0781-1787 : Diclofenac Sodium 50 mg Delayed Release Tablet


NDC: 0781-1787
Labeler: Sandoz Inc
Product Type: Human Prescription Drug
Drug Name:  Diclofenac Sodium
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA074376
Rev. Date: 


Appearance:


Markings: GG738
Shapes:  Round
Colors:  Brown
Size (mm): 10
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.

GG738: (0781-1787) Diclofenac Sodium 50 mg Delayed Release Tablet by Sandoz 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:

  • 0781-1787-01: 100 TABLET, DELAYED RELEASE IN 1 BOTTLE (0781‑1787‑01)
  • 0781-1787-10: 1000 TABLET, DELAYED RELEASE IN 1 BOTTLE (0781‑1787‑10)
  • 0781-1787-13: 10 BLISTER PACK IN 1 CARTON (0781‑1787‑13) > 10 TABLET, DELAYED RELEASE IN 1 BLISTER PACK
  • 0781-1787-60: 60 TABLET, DELAYED RELEASE IN 1 BOTTLE (0781‑1787‑60)

Active Ingredients:

  • Diclofenac Sodium

Dosage Strength:

  • 50 mg

Inactive Ingredients:

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

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 0781-1381 Diclofenac Sodium 100 mg 24 Hr Extended Release Tablet by Sandoz Inc
  • 0781-1785 Diclofenac Sodium 25 mg Delayed Release Tablet by Sandoz Inc
  • 0781-1789 Diclofenac Sodium 75 mg Delayed Release Tablet by Sandoz Inc
  • 0054-4223 Diclofenac Sodium 25 mg Delayed Release Tablet by Boehringer Ingelheim Roxane Laboratories
  • 0054-8221 Diclofenac Sodium 50 mg Delayed Release Tablet by Boehringer Ingelheim Roxane Laboratories
  • 0054-8222 Diclofenac Sodium 75 mg Delayed Release Tablet by Boehringer Ingelheim Roxane Laboratories
  • 0093-1041 Diclofenac Sodium 100 mg 24 Hr Extended Release Tablet by Teva Pharmaceuticals USA Inc.
  • 0115-1483 Diclofenac Sodium 30 mg/g Topical Gel by Global Pharmaceuticals, Division of Impax Laboratories Inc.
  • 0168-0803 Diclofenac Sodium 30 mg/g Topical Gel by E. Fougera & Co. a Division of Fougera Pharmaceuticals Inc.
  • 0168-0844 Diclofenac Sodium 30 mg/g Topical Gel by E. Fougera & Co. a Division of Fougera Pharmaceuticals Inc.
  • 0228-2550 Diclofenac Sodium 50 mg Delayed Release Tablet by Actavis Elizabeth LLC
  • 0228-2551 Diclofenac Sodium 75 mg Delayed Release Tablet by Actavis Elizabeth LLC
  • 0228-2717 Diclofenac Sodium 100 mg 24 Hr Extended Release Tablet by Actavis Elizabeth LLC
  • 0363-1210 Diclofenac Sodium 10 mg/g Topical Gel by Walgreens
  • 0363-1871 Diclofenac Sodium 10 mg/g Topical Gel by Walgreen Company
  • 0378-0355 Diclofenac Sodium 100 mg 24 Hr Extended Release Tablet by Mylan Pharmaceuticals Inc.
  • 0378-6280 Diclofenac Sodium 50 mg Delayed Release Tablet by Mylan Pharmaceuticals Inc.
  • 0378-6281 Diclofenac Sodium 75 mg Delayed Release Tablet by Mylan Pharmaceuticals Inc.
  • 0378-8750 Diclofenac Sodium 10 mg/g Topical Gel by Mylan Pharmaceuticals Inc.
  • 0472-1783 Diclofenac Sodium 30 mg/g Topical Gel by Actavis Pharma, Inc.
  • More related products ...

NDC QR Code

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NDC 0781-1787 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.