NDC 64950-214 – Meperidine Hydrochloride
Meperidine Hydrochloride 50 mg/1 · Tablet · Oral
Product NDC64950-214
Product details
- Brand name
- Meperidine Hydrochloride
- Generic name
- Meperidine Hydrochloride
- Labeler
- Genus Lifesciences Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA040893
- Marketed since
- February 14, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Meperidine Hydrochloride 50 mg/1
Uses, dosage, side effects and warnings for Meperidine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 64950-214-01 | 100 TABLET in 1 BOTTLE, PLASTIC (64950-214-01) | Feb 14, 2024 |
| 64950-214-03 | 30 TABLET in 1 BOTTLE, PLASTIC (64950-214-03) | Feb 14, 2024 |
Other Meperidine Hydrochloride products
- 42806-050 Meperidine Hydrochloride 50 mg/1 · Tablet · EPIC PHARMA, LLC
- 42806-051 Meperidine Hydrochloride 100 mg/1 · Tablet · EPIC PHARMA, LLC
- 0054-3545 Meperidine Hydrochloride 50 mg/5mL · Solution · Hikma Pharmaceuticals USA Inc.
- 0641-6052 Meperidine Hydrochloride 25 mg/mL · Injection · Hikma Pharmaceuticals USA Inc.
- 0641-6053 Meperidine Hydrochloride 50 mg/mL · Injection · Hikma Pharmaceuticals USA Inc.
- 0641-6054 Meperidine Hydrochloride 100 mg/mL · Injection · Hikma Pharmaceuticals USA Inc.