49884-231 : Praziquantel 600 mg Oral Tablet
| NDC: | 49884-231 |
| Labeler: | Par Pharmaceutical, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Praziquantel |
| Dosage Form: | Oral Tablet |
| Application #: | ANDA208820 |
| Rev. Date: |
Appearance:
| Markings: | PAR;231 |
| Shapes: |
Rectangle (4 sides) |
| Colors: |
 White |
| Size (mm): | 22 |
| Segments: * | 4 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 4 indicates a scored pill which can be broken into 4 equal pieces. | |
NDC Package Codes:
- 49884-231-83: 6 TABLET IN 1 BOTTLE (49884‑231‑83)
Active Ingredients:
- Praziquantel
Dosage Strength:
- 600 mg
Inactive Ingredients:
- Starch, Corn
- Croscarmellose Sodium
- Magnesium Stearate
- Microcrystalline Cellulose
- Povidone
- Sodium Lauryl Sulfate
- Polyethylene Glycol 1000
- Titanium Dioxide
- Hypromellose 2208 (100 Mpa.s) /
Pharmaceutical Classes:
- Antihelminthic [EPC]
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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.