0178-0901 : Thiola Ec 300 mg Oral Tablet, Delayed Release


NDC: 0178-0901
Labeler: Mission Pharmacal Company
Product Type: Human Prescription Drug
Drug Name:  Thiola Ec
Dosage Form: Oral Tablet, Delayed Release
Application #: NDA211843
Rev. Date: 


Appearance:


Markings: T3
Shapes:  Round
Colors:  White
Size (mm): 11
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:

  • 0178-0901-90: 90 TABLET, DELAYED RELEASE IN 1 BOTTLE (0178‑0901‑90)

Active Ingredients:

  • Tiopronin

Dosage Strength:

  • 300 mg

Inactive Ingredients:

  • Lactose Monohydrate
  • Hydroxypropyl Cellulose, Unspecified
  • Hydroxypropyl Cellulose, Low Substituted
  • Hypromellose, Unspecified
  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Talc
  • Triethyl Citrate
  • Magnesium Stearate /

Pharmaceutical Classes:

  • Cystine Disulfide Reduction [MoA]
  • N-substituted Glycines [CS]
  • Reducing and Complexing Thiol [EPC]

Related Products:

Based on records with the same trade name.
  • 0178-0902 Thiola Ec 100 mg Oral Tablet, Delayed Release by Mission Pharmacal Company

NDC QR Code

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NDC 0178-0901 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.