61314-245 : Betaxolol Hydrochloride 5.6 mg/ml Ophthalmic Solution/ Drops


NDC: 61314-245
Labeler: Falcon Pharmaceuticals, Ltd.
Product Type: Human Prescription Drug
Drug Name:  Betaxolol Hydrochloride
Dosage Form: Ophthalmic Solution/ Drops
Application #: NDA019270
Rev. Date: 


NDC Package Codes:

  • 61314-245-01: 5 ML IN 1 BOTTLE, PLASTIC (61314‑245‑01)
  • 61314-245-02: 15 ML IN 1 BOTTLE, PLASTIC (61314‑245‑02)
  • 61314-245-03: 10 ML IN 1 BOTTLE, PLASTIC (61314‑245‑03)

Active Ingredients:

  • Betaxolol Hydrochloride

Dosage Strength:

  • 5.6 mg/mL

Pharmaceutical Classes:

  • Adrenergic beta-Antagonists [MoA]
  • beta-Adrenergic Blocker [EPC]

Related Products:

Based on records with the same trade name.
  • 10702-013 Betaxolol Hydrochloride 10 mg (Betaxolol 8.94 mg) Oral Tablet by Kvk-tech, Inc.
  • 10702-014 Betaxolol Hydrochloride (Betaxolol 17.88 mg) Oral Tablet by Kvk-tech, Inc.

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 61314-245 QR Code

< Prev: 61314-238Next: 61314-246 >




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.