61919-181 : Paroxetine Hydrochloride Anhydrous 20 mg Oral Tablet, Film Coated
| NDC: | 61919-181 |
| Labeler: | Direct Rx |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Paroxetine Hydrochloride Anhydrous |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | ANDA075356 |
| Rev. Date: |
Appearance:
| Markings: | APO;083 |
| Shapes: |
Oval |
| Colors: |
 White |
| Size (mm): | 11 |
| Segments: * | 2 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces. | |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 61919-181-30: 30 TABLET, FILM COATED IN 1 BOTTLE (61919‑181‑30)
- 61919-181-60: 60 TABLET, FILM COATED IN 1 BOTTLE (61919‑181‑60)
- 61919-181-90: 90 TABLET, FILM COATED IN 1 BOTTLE (61919‑181‑90)
Active Ingredients:
- Paroxetine Hydrochloride Anhydrous
Dosage Strength:
- 20 mg
Inactive Ingredients:
- Anhydrous Lactose
- Hydroxypropyl Cellulose
- Hypromelloses
- Magnesium Stearate
- Polyethylene Glycols
- Sodium Starch Glycolate Type a Potato
- Titanium Dioxide
Pharmaceutical Classes:
- Serotonin Reuptake Inhibitor [EPC]
- Serotonin Uptake 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.