NDC 71335-3139 – Meclizine Hydrochloride
Meclizine Hydrochloride 12.5 mg/1 · Tablet · Oral
Product NDC71335-3139
Product details
- Brand name
- Meclizine Hydrochloride
- Generic name
- Meclizine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA010721
- Marketed since
- January 15, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Antiemetic
Active ingredients
- Meclizine Hydrochloride 12.5 mg/1
Uses, dosage, side effects and warnings for Meclizine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 71335-3139-1 | 1000 TABLET in 1 BOTTLE (71335-3139-1) | May 27, 2026 |
Other Meclizine Hydrochloride products
- 50090-7416 Meclizine Hydrochloride 25 mg/1 · Tablet · A-S Medication Solutions
- 50090-7417 Meclizine Hydrochloride 25 mg/1 · Tablet · A-S Medication Solutions
- 50090-5727 Meclizine Hydrochloride 25 mg/1 · Tablet · A-S Medication Solutions
- 50090-5728 Meclizine Hydrochloride 25 mg/1 · Tablet · A-S Medication Solutions
- 80425-0494 Meclizine Hydrochloride 25 mg/1 · Tablet · Advanced Rx of Tennessee, LLC
- 60687-730 Meclizine Hydrochloride 25 mg/1 · Tablet · American Health Packaging
- 60687-775 Meclizine Hydrochloride 12.5 mg/1 · Tablet · American Health Packaging
- 65162-444 Meclizine Hydrochloride 50 mg/1 · Tablet · Amneal Pharmaceuticals LLC
- 65162-441 Meclizine Hydrochloride 12.5 mg/1 · Tablet · Amneal Pharmaceuticals LLC
- 65162-442 Meclizine Hydrochloride 25 mg/1 · Tablet · Amneal Pharmaceuticals LLC
- 53746-441 Meclizine Hydrochloride 12.5 mg/1 · Tablet · Amneal Pharmaceuticals of New York LLC
- 53746-442 Meclizine Hydrochloride 25 mg/1 · Tablet · Amneal Pharmaceuticals of New York LLC