NDC 68180-645 – Paroxetine
Paroxetine Hydrochloride Hemihydrate 37.5 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC68180-645
Product details
- Brand name
- Paroxetine
- Generic name
- Paroxetine
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA204134
- Marketed since
- March 6, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Paroxetine Hydrochloride Hemihydrate 37.5 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68180-645-06 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68180-645-06) | Mar 6, 2017 |
Recalls mentioning this NDC
- D-0974-2017 Jul 19, 2017 · Class III
Failed Dissolution Specifications: out of specification observed in dissolution testing at 3 month long term stability study.
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