61314-238 : Carteolol Hydrochloride 10 mg/ml Ophthalmic Solution


NDC: 61314-238
Labeler: Sandoz Inc.
Product Type: Human Prescription Drug
Drug Name:  Carteolol Hydrochloride
Dosage Form: Ophthalmic Solution
Application #: ANDA075476
Rev. Date: 


NDC Package Codes:

  • 61314-238-05: 5 ML IN 1 BOTTLE, PLASTIC (61314‑238‑05)
  • 61314-238-10: 10 ML IN 1 BOTTLE, PLASTIC (61314‑238‑10)
  • 61314-238-15: 15 ML IN 1 BOTTLE, PLASTIC (61314‑238‑15)

Active Ingredients:

  • Carteolol Hydrochloride

Dosage Strength:

  • 10 mg/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 24208-367 Carteolol Hydrochloride 10 mg/ml Ophthalmic Solution/ Drops by Bausch & Lomb Incorporated
  • 45865-859 Carteolol Hydrochloride 10 mg/ml Ophthalmic Solution/ Drops by Medsource Pharmaceuticals

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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.