51079-889 : Pentoxifylline 400 mg Extended Release Tablet


NDC51079-889
Labeler: Udl Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name:  Pentoxifylline
Dosage Form: Oral Tablet, Film Coated, Extended Release
Application #: ANDA074425
Rev. Date: 


Appearance:


Markings: MYLAN;357
Shapes:  Capsule
Colors:  Purple
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.

MYLAN 357: (51079-889) Pentoxifylline 400 mg Extended Release Tablet by Udl Laboratories, 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:

  • 51079-889-19: 25 BLISTER PACK IN 1 BOX, UNIT‑DOSE (51079‑889‑19) > 1 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BLISTER PACK (51079‑889‑17)
  • 51079-889-20: 100 BLISTER PACK IN 1 BOX, UNIT‑DOSE (51079‑889‑20) > 1 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BLISTER PACK (51079‑889‑01)

Active Ingredients:

  • Pentoxifylline

Dosage Strength:

  • 400 mg

Inactive Ingredients:

  • D&c Red No. 30
  • Fd&c Blue No. 2
  • Fd&c Yellow No. 6
  • Hydroxyethyl Cellulose (140 Cps At 5%)
  • Hypromelloses
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Polydextrose
  • Polyethylene Glycol
  • Povidone
  • Titanium Dioxide
  • Triacetin

Pharmaceutical Classes:

  • Blood Viscosity Reducer [EPC]
  • Hematologic Activity Alteration [PE]

Related Products:

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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.