70121-2537 : Leuprolide AcetateLeuprolide Acetate Subcutaneous Kit
NDC: | 70121-2537 |
Labeler: | Amneal Pharmaceuticals LLC |
Product Type: | Human Prescription Drug |
Drug Name: | Leuprolide Acetate |
Dosage Form: | Subcutaneous Kit |
Application #: | ANDA215336 |
Rev. Date: |
NDC Package Codes:
- 70121-2537-6: 1 KIT IN 1 CARTON (70121‑2537‑6) * 1 VIAL, MULTI‑DOSE IN 1 CARTON (70121‑1695‑2) > 2.8 ML IN 1 VIAL, MULTI‑DOSE * 1 ML IN 1 PACKET (70121‑2538‑9)
Related Products:
Based on records with the same trade name.- 0185-7400 Leuprolide Acetate 1 mg/.2ml Subcutaneous Injection, Solution by Eon Labs, Inc.
- 0703-4014 Leuprolide Acetate 1 mg/.2ml Subcutaneous Injection, Solution by Teva Parenteral Medicines, Inc.
- 0781-4003 Leuprolide Acetate Kit by Sandoz Inc
- 16714-572 Leuprolide AcetateLeuprolide Acetate Kit by Northstar Rxllc
- 41616-936 Leuprolide Acetate Subcutaneous Kit by Sun Pharma Global Inc.
- 47335-936 Leuprolide Acetate Kit by Sun Pharma Global Fze
- 55150-478 Leuprolide AcetateLeuprolide Acetate Kit by Auromedics Pharma LLC
- 63629-8821 Leuprolide AcetateLeuprolide Acetate Kit by Bryant Ranch Prepack
- 71288-569 Leuprolide AcetateLeuprolide Acetate Subcutaneous Kit by Meitheal Pharmaceuticals Inc
- 72603-344 Leuprolide AcetateLeuprolide Acetate Kit by Northstar Rxllc
- 72664-611 Leuprolide AcetateLeuprolide Acetate Kit by Vgyaan Pharmaceuticals LLC
NDC QR Code
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Leuprolide Side Effects
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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.