83703-534 : Ifosfamide 1 g/20ml Intravenous Injection, Powder, for Solution
NDC: | 83703-534 |
Labeler: | Bamboo Us Biidco Lcc |
Product Type: | Human Prescription Drug |
Drug Name: | Ifosfamide |
Dosage Form: | Intravenous Injection, Powder, for Solution |
Application #: | NDA019763 |
Rev. Date: |
NDC Package Codes:
- 83703-534-01: 1 VIAL, SINGLE‑DOSE IN 1 CARTON (83703‑534‑01) / 20 ML IN 1 VIAL, SINGLE‑DOSE (83703‑534‑82)
Active Ingredients:
- Ifosfamide
Dosage Strength:
- 1 g/20mL
Pharmaceutical Classes:
- Alkylating Activity [MoA]
- Alkylating Drug [EPC]
Related Products:
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- 0069-4495 Ifosfamide 50 mg/ml Intravenous Injection, Solution by Pfizer Laboratories Div Pfizer Inc.
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- 0143-9531 Ifosfamide 50 mg/ml Intravenous Injection by West-ward Pharmaceuticals Corp
- 0703-3427 Ifosfamide 1 g/20ml Intravenous Injection by Teva Parenteral Medicines, Inc.
- 0703-3429 Ifosfamide 3 g/60ml Intravenous Injection by Teva Parenteral Medicines, Inc.
- 10019-925 Ifosfamide 1 g/20ml Intravenous Injection, Powder, for Solution by Baxter Healthcare Corporation
- 10019-926 Ifosfamide 3 g/60ml Intravenous Injection, Powder, for Solution by Baxter Healthcare Corporation
- 10019-927 Ifosfamide 1 g/20ml Intravenous Injection, Powder, for Solution by Baxter Healthcare Corporation
- 10019-929 Ifosfamide 3 g/60ml Intravenous Injection, Powder, for Solution by Baxter Healthcare Corporation
- 55390-047 Ifosfamide 50 mg/ml Intravenous Injection by Bedford Laboratories
- 55390-048 Ifosfamide 50 mg/ml Intravenous Injection by Bedford Laboratories
- 63323-142 Ifosfamide 1 g/1 Intravenous Injection, Powder, Lyophilized, for Solution by Fresenius Kabi USA, LLC
- 63323-174 Ifosfamide 50 mg/ml Intravenous Injection, Solution by App Pharmaceuticals, LLC
- 67457-429 Ifosfamide 50 mg/ml Intravenous Injection, Solution by Mylan Institutional LLC
- 67457-443 Ifosfamide 50 mg/ml Intravenous Injection, Solution by Mylan Institutional LLC
- 67457-609 Ifosfamide 50 mg/ml Intravenous Injection, Solution by Mylan Institutional LLC
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Ifosfamide 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.