48792-7870 : Azithromycin Monohydrate 500 mg Oral Tablet, Film Coated


NDC: 48792-7870
Labeler: Sunshine Lake Pharma Co., Ltd.
Product Type: Human Prescription Drug
Drug Name:  Azithromycin Monohydrate
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA209044
Rev. Date: 


Appearance:


Markings: L95
Shapes:  Capsule
Colors:  White
Size (mm): 17
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:

  • 48792-7870-1: 30 TABLET, FILM COATED IN 1 BOTTLE (48792‑7870‑1)

Active Ingredients:

  • Azithromycin Monohydrate

Dosage Strength:

  • 500 mg

Inactive Ingredients:

  • Talc
  • Croscarmellose Sodium
  • Magnesium Stearate
  • Sodium Lauryl Sulfate
  • Hypromellose, Unspecified
  • Polyethylene Glycol, Unspecified
  • Titanium Dioxide
  • Starch, Corn
  • Cellulose, Microcrystalline
  • Silicon Dioxide /

Pharmaceutical Classes:

  • Macrolide Antimicrobial [EPC]
  • Macrolides [CS]

Related Products:

Based on records with the same trade name.
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  • 0904-6708 Azithromycin Monohydrate 250 mg Oral Tablet by Major Pharmaceuticals
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  • 43063-715 Azithromycin Monohydrate 500 mg Oral Tablet by Pd-rx Pharmaceuticals, Inc.
  • 43063-728 Azithromycin Monohydrate 250 mg Oral Tablet by Pd-rx Pharmaceuticals, Inc.
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  • 50436-3136 Azithromycin Monohydrate 500 mg Oral Tablet by Unit Dose Services
  • 53002-3221 Azithromycin Monohydrate 500 mg Oral Tablet by Rpk Pharmaceuticals, Inc.
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  • 57297-160 Azithromycin Monohydrate 250 mg Oral Tablet by Lupin Limited
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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.