Prevents severely restricted mobility during acute illness. ANDA 214646, held by Be Pharms. Enoxaparin Sodium.
As of Nov 15, 2026, ANDA 214646 (Enoxaparin Sodium (Preservative Free)), held by Be Pharms, was first approved by FDA on Jun 6, 2023, with 0 approved supplements and 0 published complete response letters.
Enoxaparin sodium injection is a low molecular weight heparin (LMWH) indicated for:
| Date | Submission | Status | Documents |
|---|---|---|---|
| Jun 6, 2023 | Original application | Approved | None posted |
| Enoxaparin Sodium (Preservative Free)30MG/0.3ML (100MG/ML) · injectable;subcutaneous | Enoxaparin Sodium | Rx |
| Enoxaparin Sodium (Preservative Free)40MG/0.4ML (100MG/ML) · injectable;subcutaneous | Enoxaparin Sodium | Rx |
| Enoxaparin Sodium (Preservative Free)60MG/0.6ML (100MG/ML) · injectable;subcutaneous | Enoxaparin Sodium | Rx |
| Enoxaparin Sodium (Preservative Free)80MG/0.8ML (100MG/ML) · injectable;subcutaneous | Enoxaparin Sodium | Rx |
| Enoxaparin Sodium (Preservative Free)100MG/ML (100MG/ML) · injectable;subcutaneous | Enoxaparin Sodium | Rx |
| Enoxaparin Sodium (Preservative Free)120MG/0.8ML (150MG/ML) · injectable;subcutaneous | Enoxaparin Sodium | Rx |
| Enoxaparin Sodium (Preservative Free)150MG/ML (150MG/ML) · injectable;subcutaneous | Enoxaparin Sodium | Rx |
Approvals, supplements, products and documents come from FDA's Drugs@FDA data files, refreshed daily; Drugs@FDA lists approved applications only. Complete response letters are FDA's published letters. Drugs@FDA and FDA complete response letters