ANDA 80784, held by Purepac Pharm. Folic Acid.
As of Nov 15, 2026, ANDA 80784 (Folic Acid), held by Purepac Pharm, was first approved by FDA on Nov 2, 1972, with 1 approved supplement and 0 published complete response letters.
| Date | Submission | Status | Documents |
|---|---|---|---|
| Nov 2, 1972 | Original application | Approved |
| Product | Active ingredient | Marketing |
|---|---|---|
| Folic Acid1MG ยท tablet;oral | Folic Acid | Discontinued |
| Jan 17, 1973 | Supplement 1 | Approved | |
| Nov 2, 1972 | Original application | Approved |
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
