67386-601 : Peganone 250 mg Oral Tablet
| NDC: | 67386-601 |
| Labeler: | Lundbeck Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Peganone |
| Dosage Form: | Oral Tablet |
| Application #: | NDA010841 |
| Rev. Date: |
Appearance:
| Markings: | OV;61 |
| Shapes: |
Round |
| 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. | |
NDC Package Codes:
- 67386-601-01: 100 TABLET IN 1 BOTTLE (67386‑601‑01)
Active Ingredients:
- Ethotoin
Dosage Strength:
- 250 mg
Inactive Ingredients:
- Acacia
- Lactose
- Carboxymethylcellulose Sodium
- Stearic Acid
- Talc
Pharmaceutical Classes:
- Anti-epileptic Agent [EPC]
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
Related Products:
Based on records with the same trade name.- 55292-601 Peganone 250 mg Oral Tablet by Recordati Rare Diseases, Inc.
- 55292-602 Peganone 250 mg Oral Tablet by Recordati Rare Diseases, Inc.
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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.