65862-310 : Didanosine 125 mg Delayed Release Capsule


NDC65862-310
Labeler: Aurobindo Pharma Limited
Product Type: Human Prescription Drug
Drug Name: Didanosine
Dosage Form: Oral Capsule, Delayed Release
Application #: ANDA090094
Rev. Date: 


Appearance:


Markings: D;70
Shapes:  Capsule
Colors:  White
Size (mm): 16
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:

  • 65862-310-05: 500 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (65862‑310‑05)
  • 65862-310-14: 10 BLISTER PACK IN 1 CARTON (65862‑310‑14) > 14 CAPSULE, DELAYED RELEASE IN 1 BLISTER PACK
  • 65862-310-30: 30 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (65862‑310‑30)

Active Ingredients:

  • Didanosine

Dosage Strength:

  • 125 mg

Inactive Ingredients:

  • Sodium Starch Glycolate Type a Potato
  • Carboxymethylcellulose Sodium
  • Sodium Lauryl Sulfate
  • Hypromellose 2910 (3 Mpa.s)
  • Talc
  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Diethyl Phthalate
  • Silicon Dioxide
  • Gelatin
  • Titanium Dioxide
  • Ferrosoferric Oxide
  • Shellac

Pharmaceutical Classes:

  • Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
  • Nucleoside Analog [EXT]
  • Nucleoside Reverse Transcriptase Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
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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.