0187-0453 : Zelapar 1.25 mg Disintegrating Tablet
NDC: | 0187-0453 |
Labeler: | Valeant Pharmaceuticals International |
Product Type: | Human Prescription Drug |
Drug Name: | Zelapar |
Dosage Form: | Oral Tablet |
Application #: | NDA021479 |
Rev. Date: |
Appearance:
Markings: | V |
Shapes: |
Round |
Colors: |
Yellow |
Size (mm): | 12 |
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:
- 0187-0453-02: 6 POUCH IN 1 CARTON (0187‑0453‑02) > 1 BLISTER PACK IN 1 POUCH > 10 TABLET IN 1 BLISTER PACK
- 0187-0453-03: 1 POUCH IN 1 CARTON (0187‑0453‑03) > 10 TABLET, ORALLY DISINTEGRATING IN 1 POUCH
Active Ingredients:
- Selegiline Hydrochloride
Dosage Strength:
- 1.25 mg
Inactive Ingredients:
- Gelatin
- Mannitol
- Glycerin
- Aspartame
- Citric Acid Monohydrate
- Ferric Oxide Yellow
Pharmaceutical Classes:
- Monoamine Oxidase Inhibitor [EPC]
- Monoamine Oxidase Inhibitors [MoA]
- Monoamine Oxidase Type B Inhibitor [EPC]
- Monoamine Oxidase-B Inhibitors [MoA]
NDC QR Code
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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.