70786-2550 : Diclofenac Sodium 50 mg Oral Tablet, Delayed Release


NDC: 70786-2550
Labeler: Unit Dose Services
Product Type: Human Prescription Drug
Drug Name:  Diclofenac Sodium
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA074514
Rev. Date: 


Appearance:


Markings: R;550
Shapes:  Round
Colors:  White
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.

R 550: (0228-2550) Diclofenac Sodium 50 mg Oral Tablet, Delayed Release by Unit Dose Services
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:

  • 70786-2550-1: 30 TABLET, DELAYED RELEASE IN 1 BOTTLE (70786‑2550‑1)
  • 70786-2550-2: 60 TABLET, DELAYED RELEASE IN 1 BOTTLE (70786‑2550‑2)

Active Ingredients:

  • Diclofenac Sodium

Dosage Strength:

  • 50 mg

Inactive Ingredients:

  • Hypromelloses
  • Lactose Monohydrate
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Polyethylene Glycols
  • Polysorbate 80
  • Propylene Glycol
  • Silicon Dioxide
  • Sodium Alginate
  • Sodium Starch Glycolate Type a Potato
  • Stearic Acid
  • Ferrosoferric Oxide
  • Talc
  • Titanium Dioxide
  • Polyvinyl Acetate Phthalate
  • Aluminum Hydroxide

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.
  • 70786-0201 Diclofenac Sodium 75 mg Oral Tablet, Delayed Release by Unit Dose Services
  • 50436-0002 Diclofenac Sodium 16.05 mg/ml Topical Solution by Unit Dose Services
  • 50436-0355 Diclofenac Sodium 30 mg/g Topical Gel by Unit Dose Services
  • 50436-0676 Diclofenac Sodium 100 mg Oral Tablet, Film Coated, Extended Release by Unit Dose Services
  • 50436-0833 Diclofenac Sodium 10 mg/g Topical Gel by Unit Dose Services
  • 50436-1182 Diclofenac Sodium 50 mg Delayed Release Tablet by Unit Dose Services
  • 50436-2201 Diclofenac Sodium 75 mg Oral Tablet, Delayed Release by Unit Dose Services
  • 50436-3339 Diclofenac Sodium 16.05 mg/ml Topical Solution by Unit Dose Services
  • 50436-3340 Diclofenac Sodium 16.05 mg/ml Topical Solution by Unit Dose Services
  • 50436-3990 Diclofenac Sodium 16.05 mg/ml Topical Solution by Unit Dose Services
  • 50436-6924 Diclofenac Sodium 75 mg Delayed Release Tablet by Unit Dose Services
  • 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
  • More related products ...

NDC QR Code

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NDC 70786-2550 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.