16571-889 : Fluphenazine Hydrochoride 1 mg Oral Tablet, Film Coated


NDC: 16571-889
Labeler: Rising Pharma Holdings, Inc.
Product Type: Human Prescription Drug
Drug Name:  Fluphenazine Hydrochoride
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA218283
Rev. Date: 


NDC Package Codes:

  • 16571-889-09: 90 TABLET, FILM COATED IN 1 CONTAINER (16571‑889‑09)
  • 16571-889-50: 500 TABLET, FILM COATED IN 1 CONTAINER (16571‑889‑50)

Active Ingredients:

  • Fluphenazine Hydrochloride

Dosage Strength:

  • 1 mg

Pharmaceutical Classes:

  • Phenothiazine [EPC]
  • Phenothiazines [CS]

Related Products:

Based on records with the same trade name.
  • 16571-890 Fluphenazine Hydrochoride 2.5 mg Oral Tablet, Film Coated by Rising Pharma Holdings, Inc.
  • 16571-891 Fluphenazine Hydrochoride 5 mg Oral Tablet, Film Coated by Rising Pharma Holdings, Inc.
  • 16571-892 Fluphenazine Hydrochoride 10 mg Oral Tablet, Film Coated by Rising Pharma Holdings, Inc.

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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.