NDC 70121-2537 – Leuprolide acetate
· Kit · Subcutaneous
Product NDC70121-2537
Product details
- Brand name
- Leuprolide acetate
- Generic name
- Leuprolide acetate
- Labeler
- Amneal Pharmaceuticals LLC
- Dosage form
- Kit
- Route
- Subcutaneous
- Marketing category
- ANDA · ANDA215336
- Marketed since
- November 7, 2022
- Listing expires
- December 31, 2027
Active ingredients
Uses, dosage, side effects and warnings for Leuprolide Acetate →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70121-2537-6 | 1 KIT in 1 CARTON (70121-2537-6) * 1 VIAL, MULTI-DOSE in 1 CARTON (70121-1695-2) / 2.8 mL in 1 VIAL, MULTI-DOSE * 1 mL in 1 PACKET (70121-2538-9) | Nov 7, 2022 |
Other Leuprolide Acetate products
- 55150-478 · Kit · Eugia US LLC
- 71288-569 · Kit · Meitheal Pharmaceuticals Inc
- 72603-344 · Kit · NorthStar RxLLC
- 0121-2106 · Kit · PAI Holdings, LLC dba PAI Pharma
- 0781-4003 · Kit · Sandoz Inc
- 47335-936 · Kit · Sun Pharmaceutical Industries, Inc.
- 72843-591 · Kit · UBI Pharma Inc.
- 72664-611 · Kit · VGYAAN Pharmaceuticals LLC
- 70771-1687 · Kit · Zydus Lifesciences Limited
- 70710-1769 · Kit · Zydus Pharmaceuticals USA Inc.
- 42023-259 Leuprolide Acetate 1 mg/.2mL · Injection · Endo USA, Inc.