49884-732 : Sumycin 250 mg Oral Tablet, Film Coated


NDC: 49884-732
Labeler: Par Pharmaceutical, Inc.
Product Type: Human Prescription Drug
Drug Name:  Sumycin
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA061147
Rev. Date: 


Appearance:


Markings: 732
Shapes:  Oval
Colors:  Pink
Size (mm): 13
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:

  • 49884-732-01: 100 TABLET, FILM COATED IN 1 BOTTLE (49884‑732‑01)
  • 49884-732-10: 1000 TABLET, FILM COATED IN 1 BOTTLE (49884‑732‑10)

Active Ingredients:

  • Tetracycline Hydrochloride

Dosage Strength:

  • 250 mg

Inactive Ingredients:

  • Anhydrous Lactose
  • Magnesium Stearate
  • Microcrystalline Cellulose
  • Povidone
  • Starch, Pregelatinized Corn
  • Stearic Acid
  • D&c Red No. 30
  • Hypromellose, Unspecified
  • Titanium Dioxide
  • Triacetin

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 49884-733 Sumycin 500 mg Oral Tablet, Film Coated by Par Pharmaceutical, Inc.

NDC QR Code

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NDC 49884-732 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.