17224-840 : Lomaira 8 mg Oral Tablet


NDC: 17224-840
Labeler: Calvin Scott & Co., Inc.
Product Type: Human Prescription Drug
Drug Name:  Lomaira
Dosage Form: Oral Tablet
Application #: ANDA203495
Rev. Date: 
CSA Schedule: CIV (US) [1]


[1] Schedule IV Controlled Substance: Low potential for abuse relative to substances in Schedule III. Examples include Alprazolam (Xanax), Diazepam (Valium), Carisoprodol (Soma), Clonazepam (Klonopin), Lorazepam (Ativan), Clorazepate (Tranxene), Midazolam (Versed), Temazepam (Restoril), and Triazolam (Halcion).. More Details: US Dept of Justice Controlled Substance Schedules.

NDC Package Codes:

  • 17224-840-28: 28 TABLET IN 1 BOTTLE (17224‑840‑28)
  • 17224-840-60: 60 TABLET IN 1 BOTTLE (17224‑840‑60)
  • 17224-840-90: 90 TABLET IN 1 BOTTLE (17224‑840‑90)

Active Ingredients:

  • Phentermine Hydrochloride

Dosage Strength:

  • 8 mg

Pharmaceutical Classes:

  • Appetite Suppression [PE]
  • Increased Sympathetic Activity [PE]
  • Sympathomimetic Amine Anorectic [EPC]

Related Products:

Based on records with the same trade name.
  • 10702-001 Lomaira 8 mg Oral Tablet by Kvk-tech, Inc.
  • 63629-7874 Lomaira 8 mg Oral Tablet by Bryant Ranch Prepack

NDC QR Code

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NDC 17224-840 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.