52125-870 : Ondansetron Hydrochloride 4 mg Oral Tablet, Film Coated
| NDC: | 52125-870 |
| Labeler: | Remedyrepack Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Ondansetron Hydrochloride |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | ANDA077050 |
| Rev. Date: |
Appearance:
| Markings: | 130 |
| Shapes: |
Oval |
| Colors: |
 White |
| Size (mm): | 10 |
| Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. | |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 52125-870-02: 30 TABLET, FILM COATED IN 1 BLISTER PACK (52125‑870‑02)
Active Ingredients:
- Ondansetron Hydrochloride
Dosage Strength:
- 4 mg
Inactive Ingredients:
- Anhydrous Lactose
- Hypromelloses
- Titanium Dioxide
- Magnesium Stearate
- Cellulose, Microcrystalline
- Polyethylene Glycol 400
- Starch, Corn
Pharmaceutical Classes:
- Serotonin 3 Receptor Antagonists [MoA]
- Serotonin-3 Receptor Antagonist [EPC]
Related Products:
Based on records with the same trade name.- 52125-334 Ondansetron Hydrochloride 2 mg/ml Intramuscular Injection, Solution by Remedyrepack Inc.
- 52125-347 Ondansetron 8 mg (As Ondansetron Hydrochloride Dihydrate 10 mg) Oral Tablet by Remedyrepack Inc.
- 52125-574 Ondansetron Hydrochloride 2 mg/ml Intravenous Injection by Remedyrepack Inc.
- 52125-983 Ondansetron Hydrochloride 2 mg/ml Intravenous Solution by Remedyrepack Inc.
- 49349-714 Ondansetron 4 mg (Ondansetron Hydrochloride Dihydrate 5 mg) Oral Tablet by Remedyrepack Inc.
- 49349-810 Ondansetron 8 mg (As Ondansetron Hydrochloride Dihydrate 10 mg) Oral Tablet by Remedyrepack Inc.
- 61786-693 Ondansetron Hydrochloride 4 mg Oral Tablet, Film Coated by Remedyrepack Inc.
- 61786-699 Ondansetron Hydrochloride 8 mg Oral Tablet, Film Coated by Remedyrepack Inc.
- 70518-1042 Ondansetron Hydrochloride 4 mg Oral Tablet, Film Coated by Remedyrepack Inc.
- 70518-1394 Ondansetron Hydrochloride 8 mg Oral Tablet, Film Coated by Remedyrepack Inc.
- 70518-1585 Ondansetron Hydrochloride 4 mg Oral Tablet, Film Coated by Remedyrepack Inc.
- 70518-3511 Ondansetron Hydrochloride 8 mg Oral Tablet, Film Coated by Remedyrepack Inc.
- 0054-0064 Ondansetron Hydrochloride 4 mg/5ml Oral Solution by Roxane Laboratories, Inc
- 0069-1340 Ondansetron Hydrochloride 2 mg/ml Intramuscular; Intravenous Injection, Solution by Pfizer Laboratories Div Pfizer Inc
- 0093-0233 Ondansetron 4 mg (Ondansetron Hydrochloride Dihydrate 5 mg) Oral Tablet by Teva Pharmaceuticals USA Inc
- 0093-7236 Ondansetron 8 mg (As Ondansetron Hydrochloride Dihydrate 10 mg) Oral Tablet by Teva Pharmaceuticals USA Inc
- 0179-0099 Ondansetron 4 mg (Ondansetron Hydrochloride Dihydrate 5 mg) Oral Tablet by Kaiser Foundation Hospitals
- 0179-0100 Ondansetron 8 mg (As Ondansetron Hydrochloride Dihydrate 10 mg) Oral Tablet by Kaiser Foundation Hospitals
- 0179-0247 Ondansetron Hydrochloride 4 mg Oral Tablet, Film Coated by Kaiser Foundation Hospitals
- 0179-0248 Ondansetron Hydrochloride 8 mg Oral Tablet, Film Coated by Kaiser Foundation Hospitals
- 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.