Paxil
Paroxetine hydrochloride · Tablet, Film Coated · Oral
No FDA structured label text is available for Paxil. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Paroxetine Hydrochloride in 7 products
Paxil NDC products (7)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 60505-4377 | Paroxetine Hydrochloride 12.5 mg/1 Tablet, Film Coated, Extended Release | Apotex Corp | NDA |
| 60505-4378 | Paroxetine Hydrochloride 25 mg/1 Tablet, Film Coated, Extended Release | Apotex Corp | NDA |
| 60505-4379 | Paroxetine Hydrochloride 37.5 mg/1 Tablet, Film Coated, Extended Release | Apotex Corp | NDA |
| 60505-4517 | Paroxetine Hydrochloride 10 mg/1 Tablet, Film Coated | Apotex Corp | NDA |
| 60505-4518 | Paroxetine Hydrochloride 20 mg/1 Tablet, Film Coated | Apotex Corp | NDA |
| 60505-4519 | Paroxetine Hydrochloride 30 mg/1 Tablet, Film Coated | Apotex Corp | NDA |
| 60505-4520 | Paroxetine Hydrochloride 40 mg/1 Tablet, Film Coated | Apotex Corp | NDA |
Frequently asked questions
Who makes Paxil?
Paxil is listed by 1 labeler in the FDA NDC directory, including Apotex Corp.