24979-041 : Megestrol Acetate 125 mg/ml Oral Suspension
NDC: | 24979-041 |
Labeler: | Twi Pharmaceuticals, Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Megestrol Acetate |
Dosage Form: | Oral Suspension |
Application #: | ANDA203139 |
Rev. Date: |
NDC Package Codes:
- 24979-041-13: 150 ML IN 1 BOTTLE (24979‑041‑13)
Active Ingredients:
- Megestrol Acetate
Dosage Strength:
- 125 mg/mL
Pharmaceutical Classes:
- Progesterone Congeners [Chemical/Ingredient]
- Progestin [EPC]
Related Products:
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- 0121-4776 Megestrol Acetate 40 mg/ml Oral Suspension by Pharmaceutical Associates, Inc.
- 0555-0606 Megestrol Acetate 20 mg Oral Tablet by Barr Laboratories Inc.
- 0555-0607 Megestrol Acetate 40 mg Oral Tablet by Barr Laboratories Inc.
- 0615-3570 Megestrol Acetate 40 mg Oral Tablet by Ncs Healthcare of Ky, Inc Dba Vangard Labs
- 0904-3571 Megestrol Acetate 40 mg Oral Tablet by Major Pharmaceuticals
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- 0904-7236 Megestrol Acetate 40 mg Oral Tablet by Major Pharmaceuticals
- 17856-0060 Megestrol Acetate 40 mg/ml Oral Suspension by Atlantic Biologicals Corp.
- 17856-0907 Megestrol Acetate 40 mg/ml Oral Suspension by Atlantic Biologicals Corps
- 33358-903 Megestrol Acetate 40 mg/ml Oral Suspension by Rxchange Co
- 42291-588 Megestrol Acetate 125 mg/ml Oral Suspension by Avkare, Inc.
- 43826-061 Megestrol Acetate 125 mg/ml Oral Suspension by Bora Pharmaceutical Laboratories Inc.
- 49884-230 Megestrol Acetate 125 mg/ml Oral Suspension by Par Pharmaceutical, Inc.
- More related products ...
NDC QR Code
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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.