23155-611 : Doxycycline Hyclate Delayed Release 200 mg Oral Tablet, Delayed Release


NDC: 23155-611
Labeler: Heritage Pharmaceuticals Inc.
Product Type: Human Prescription Drug
Drug Name: Doxycycline Hyclate Delayed Release
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA200856
Rev. Date: 


Appearance:


Markings: I1;18
Shapes:  Oval
Colors:  White
Size (mm): 20
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:

  • 23155-611-04: 250 TABLET, DELAYED RELEASE IN 1 BOTTLE (23155‑611‑04)
  • 23155-611-06: 60 TABLET, DELAYED RELEASE IN 1 BOTTLE (23155‑611‑06)

Active Ingredients:

  • Doxycycline Hyclate

Dosage Strength:

  • 200 mg

Inactive Ingredients:

  • Lactose Monohydrate
  • Cellulose, Microcrystalline
  • Sodium Lauryl Sulfate
  • Sodium Chloride
  • Hypromellose Phthalate (31% Phthalate, 40 Cst)
  • Hypromellose 2910 (5 Mpa.s)
  • Triethyl Citrate
  • Anhydrous Lactose
  • Crospovidone (15 Mpa.s At 5%)
  • Stearic Acid
  • Magnesium Stearate
  • Hypromellose 2910 (6 Mpa.s)
  • Triacetin /

Pharmaceutical Classes:

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

NDC QR Code

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NDC 23155-611 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.