49884-254 : Tolcapone 100 1/1 Oral Tablet, Coated
| NDC: | 49884-254 |
| Labeler: | Par Pharmaceutical Companies, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Tolcapone |
| Dosage Form: | Oral Tablet, Coated |
| Application #: | ANDA204584 |
| Rev. Date: |
Appearance:
| Markings: | EP;370 |
| Shapes: |
Hexagon (6 sides) |
| Colors: |
 Brown |
| 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:
- 49884-254-09: 90 TABLET, COATED IN 1 BOTTLE (49884‑254‑09)
Active Ingredients:
- Tolcapone
Dosage Strength:
- 100 1/1
Inactive Ingredients:
- Calcium Phosphate, Dibasic, Anhydrous
- Lactose Monohydrate
- Sodium Starch Glycolate Type a Potato
- Cellulose, Microcrystalline
- Povidone K30
- Talc
- Magnesium Stearate
- Titanium Dioxide
- Polyvinyl Alcohol
- Polyethylene Glycols
- Ferric Oxide Yellow
- Ferric Oxide Red
Pharmaceutical Classes:
- Catechol O-Methyltransferase Inhibitors [MoA]
- Catechol-O-Methyltransferase Inhibitor [EPC]
Related Products:
Based on records with the same trade name.- 50742-193 Tolcapone 100 mg Oral Tablet by Ingenus Pharmaceuticals, LLC
- 68682-938 Tolcapone 100 mg Oral Tablet, Film Coated by Oceanside Pharmaceuticals
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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.