31722-046 : Diclofenac Potassium 50 mg Oral Powder, for Solution
NDC: | 31722-046 |
Labeler: | Camber Pharmaceuticals, Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Diclofenac Potassium |
Dosage Form: | Oral Powder, for Solution |
Application #: | ANDA215375 |
Rev. Date: |
NDC Package Codes:
- 31722-046-31: 1 POWDER, FOR SOLUTION IN 1 PACKET (31722‑046‑31)
- 31722-046-32: 9 POWDER, FOR SOLUTION IN 1 CARTON (31722‑046‑32)
Active Ingredients:
- Diclofenac Potassium
Dosage Strength:
- 50 mg
Pharmaceutical Classes:
- Anti-Inflammatory Agents
- Non-Steroidal [CS]
- Cyclooxygenase Inhibitors [MoA]
- Decreased Prostaglandin Production [PE]
- Nonsteroidal Anti-inflammatory Drug [EPC]
Related Products:
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- 0378-2474 Diclofenac Pot 50 mg Oral Tablet by Mylan Pharmaceuticals Inc.
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- 16590-072 Diclofenac Pot 50 mg Oral Tablet by Stat Rx USA
- 21695-838 Diclofenac Pot 50 mg Oral Tablet by Rebel Distributors Corp
- 23155-840 Diclofenac Potassium 25 mg Oral Capsule, Liquid Filled by Avet Pharmaceuticals Inc
- 24470-924 Diclofenac Potassium 25 mg Oral Tablet by Cintex Services, LLC
- 33261-038 Diclofenac Potassium 50 mg/1 Oral Tablet, Film Coated by Aidarex Pharmaceuticals LLC
- 35356-713 Diclofenac Pot 50 mg Oral Tablet by Lake Erie Medical Dba Quality Care Products LLC
- 42291-042 Diclofenac Potassium 50 mg Oral Tablet, Film Coated by Avkare
- 43063-848 Diclofenac Potassium 50 mg Oral Tablet, Film Coated by Pd-rx Pharmaceuticals, Inc.
- 49349-955 Diclofenac Pot 50 mg Oral Tablet by Remedyrepack Inc.
- 49999-593 Diclofenac Pot 50 mg Oral Tablet by Lake Erie Medical & Surgical Supply Dba Quality Care Products LLC
- 50090-0646 Diclofenac Potassium 50 mg Oral Tablet, Film Coated by A-s Medication Solutions
- 50090-0647 Diclofenac Potassium 50 mg Oral Tablet, Film Coated by A-s Medication Solutions
- 50090-1535 Diclofenac Potassium 50 mg Oral Tablet, Film Coated by A-s Medication Solutions
- 50090-5893 Diclofenac Potassium 50 mg Oral Tablet, Coated by A-s Medication Solutions
- More related products ...
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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.