43598-540 : Minolira 105 mg Oral Tablet, Extended Release


NDC43598-540
Labeler: Dr. Reddys Laboratories Inc
Product Type: Human Prescription Drug
Drug Name:  Minolira
Dosage Form: Oral Tablet, Extended Release
Application #: NDA209269
Rev. Date: 


Appearance:


Markings: M1
Shapes:  Rectangle (4 sides)
Colors:  White
Size (mm): 19
Segments: * 2

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces.

NDC Package Codes:

  • 43598-540-30: 30 TABLET, EXTENDED RELEASE IN 1 BOTTLE (43598‑540‑30)

Active Ingredients:

  • Minocycline Hydrochloride

Dosage Strength:

  • 105 mg

Inactive Ingredients:

  • Isopropyl Alcohol
  • Sodium Stearyl Fumarate
  • Talc
  • Cellulose, Microcrystalline
  • Hypromellose 2910 (5 Mpa.s)
  • Polyethylene Glycol 400
  • Ethylcellulose (10 Mpa.s)
  • Hypromellose 2910 (15 Mpa.s)
  • Triethyl Citrate
  • Hydroxypropyl Cellulose (Type H)
  • Water

Pharmaceutical Classes:

  • Tetracycline-class Drug [EPC]
  • Tetracyclines [CS]

Related Products:

Based on records with the same trade name.
  • 43598-539 Minolira 135 mg Oral Tablet, Extended Release by Dr. Reddys Laboratories Inc

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.