NDC 27241-255 – Fluphenazine hydrochloride
Fluphenazine Hydrochloride 1 mg/1 · Tablet · Oral
Product NDC27241-255
Product details
- Brand name
- Fluphenazine hydrochloride
- Generic name
- Fluphenazine hydrochloride
- Labeler
- Ajanta Pharma USA Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA217410
- Marketed since
- January 5, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Phenothiazine
Active ingredients
- Fluphenazine Hydrochloride 1 mg/1
Uses, dosage, side effects and warnings for Fluphenazine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 27241-255-01 | 100 TABLET in 1 BOTTLE (27241-255-01) | Jan 5, 2023 |
Recalls mentioning this NDC
- D-0836-2026 Sep 16, 2026 · Class III
Failed impurities/degradation specifications: (OOS) for Organic Impurities by HPLC (Impurity-A) during testing at the 18 months long term stability. Result: 1.1 percent. Spec: 1.0 percent.
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