69336-113 : Fenortho 200 mg Oral Capsule
| NDC: | 69336-113 |
| Labeler: | Sterling Knight Pharmaceuticals LLC |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Fenortho |
| Dosage Form: | Oral Capsule |
| Application #: | NDA017604 |
| Rev. Date: |
Appearance:
| Markings: | RX681 |
| Shapes: |
Capsule |
| Colors: |
 Yellow /
 White |
| Size (mm): | 23 |
| 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. | |
NDC Package Codes:
- 69336-113-10: 100 CAPSULE IN 1 BOTTLE (69336‑113‑10)
- 69336-113-90: 90 CAPSULE IN 1 BOTTLE (69336‑113‑90)
Active Ingredients:
- Fenoprofen Calcium
Dosage Strength:
- 200 mg
Inactive Ingredients:
- Crospovidone
- Magnesium Stearate
- Sodium Lauryl Sulfate
- Talc
- Gelatin
- Titanium Dioxide
- Brown Iron Oxide
Pharmaceutical Classes:
- Cyclooxygenase Inhibitors [MoA]
- Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient]
- Nonsteroidal Anti-inflammatory Drug [EPC]
Related Products:
Based on records with the same trade name.- 54288-129 Fenortho 200 mg Oral Capsule by Bpi Labs LLC
- 54288-130 Fenortho 400 mg Oral Capsule by Bpi Labs LLC
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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.