0378-6971 : Tadalfil 5 mg Oral Tablet, Film Coated


NDC: 0378-6971
Labeler: Mylan Pharmaceuticals Inc.
Product Type: Human Prescription Drug
Drug Name:  Tadalfil
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA206957
Rev. Date: 


Appearance:


Markings: M;TL;2
Shapes:  Round
Colors:  Yellow
Size (mm): 6
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:

  • 0378-6971-93: 30 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (0378‑6971‑93)

Active Ingredients:

  • Tadalafil

Dosage Strength:

  • 5 mg

Inactive Ingredients:

  • Anhydrous Lactose
  • Silicon Dioxide
  • Croscarmellose Sodium
  • Hypromellose, Unspecified
  • Lactose Monohydrate
  • Magnesium Stearate
  • Microcrystalline Cellulose
  • Poloxamer 188
  • Povidone, Unspecified
  • Sodium Lauryl Sulfate
  • Titanium Dioxide
  • Triacetin
  • Ferric Oxide Yellow /

Pharmaceutical Classes:

  • Phosphodiesterase 5 Inhibitor [EPC]
  • Phosphodiesterase 5 Inhibitors [MoA]

NDC QR Code

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NDC 0378-6971 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.