NDC 59746-122 – Meclizine Hydrochloride
Meclizine Hydrochloride 12.5 mg/1 · Tablet · Oral
Product NDC59746-122
Product details
- Brand name
- Meclizine Hydrochloride
- Generic name
- Meclizine Hydrochloride
- Labeler
- Jubilant Cadista Pharmacuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA040659
- Marketed since
- June 4, 2010
- Marketing end
- October 31, 2026
- Pharmacologic class
- Antiemetic
Active ingredients
- Meclizine Hydrochloride 12.5 mg/1
Uses, dosage, side effects and warnings for Meclizine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 59746-122-06 | 100 TABLET in 1 BOTTLE (59746-122-06) | Jun 4, 2010 |
| 59746-122-10 | 1000 TABLET in 1 BOTTLE (59746-122-10) | Jun 4, 2010 |
Recalls mentioning this NDC
- D-0767-2022 Apr 6, 2022 · Class I
Labeling: Label mix-up: Incorrect label placed on product. Shipper cases labeled Meclizine Hydrochloride Tablets contain bottles incorrectly labeled as PredniSONE Tablets. The tablets in the bottles… - D-0082-2018 Nov 22, 2017 · Class III
Marketed without an approved NDA/ANDA: Bottles were released prior to final approval.
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