NDC 68001-436 – Cetirizine Hydrochloride (Allergy)
Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC68001-436
Product details
- Brand name
- Cetirizine Hydrochloride (Allergy)
- Generic name
- Cetirizine Hydrochloride
- Labeler
- BluePoint Laboratories
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA090760
- Marketed since
- June 19, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Cetirizine Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Cetirizine Hydrochloride (Allergy) →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68001-436-04 | 1 BOTTLE in 1 CARTON (68001-436-04) / 30 TABLET in 1 BOTTLE | Jun 19, 2020 |
| 68001-436-96 | 10 BLISTER PACK in 1 CARTON (68001-436-96) / 10 TABLET in 1 BLISTER PACK (68001-436-16) | Jun 19, 2020 |
| 68001-436-97 | 1 BOTTLE in 1 CARTON (68001-436-97) / 300 TABLET in 1 BOTTLE | Jun 19, 2020 |
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