NDC 68001-439 – Fexofenadine hydrochloride
Fexofenadine Hydrochloride 60 mg/1 · Tablet · Oral
Product NDC68001-439
Product details
- Brand name
- Fexofenadine hydrochloride
- Generic name
- Fexofenadine hydrochloride
- Labeler
- BluePoint Laboratories
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076502
- Marketed since
- June 19, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Fexofenadine Hydrochloride 60 mg/1
Uses, dosage, side effects and warnings for Fexofenadine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68001-439-00 | 1 BOTTLE in 1 CARTON (68001-439-00) / 100 TABLET in 1 BOTTLE | Jun 19, 2020 |
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