42571-264 : Tafluprost .0045 mg/.3ml Ophthalmic Solution/ Drops
NDC: | 42571-264 |
Labeler: | Micro Labs Limited |
Product Type: | Human Prescription Drug |
Drug Name: | Tafluprost |
Dosage Form: | Ophthalmic Solution/ Drops |
Application #: | ANDA209051 |
Rev. Date: |
NDC Package Codes:
- 42571-264-26: 1 POUCH IN 1 CARTON (42571‑264‑26) > 15 VIAL IN 1 POUCH > .3 ML IN 1 VIAL
- 42571-264-73: 2 POUCH IN 1 CARTON (42571‑264‑73) > 15 VIAL IN 1 POUCH > .3 ML IN 1 VIAL
- 42571-264-74: 6 POUCH IN 1 CARTON (42571‑264‑74) > 15 VIAL IN 1 POUCH > .3 ML IN 1 VIAL
Active Ingredients:
- Tafluprost
Dosage Strength:
- .0045 mg/.3mL
Pharmaceutical Classes:
- Increased Prostaglandin Activity [PE]
- Prostaglandin Analog [EPC]
- Prostaglandin Receptor Agonists [MoA]
- Prostaglandins [CS]
Related Products:
Based on records with the same trade name.- 0781-6184 Tafluprost .0045 mg/.3ml Ophthalmic Solution/ Drops by Sandoz Inc
- 65302-062 Tafluprost .0045 mg/.3ml Ophthalmic Solution by The Ritedose Corporation
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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.