Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 080816
Company: LANNETT
Company: LANNETT
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| FOLIC ACID | FOLIC ACID | 1MG | TABLET;ORAL | Discontinued | None | No | No |
Original Approvals or Tentative Approvals
| Action Date | Submission | Action Type | Submission Classification | Review Priority; Orphan Status | Letters, Reviews, Labels, Patient Package Insert | Notes | Url |
|---|---|---|---|---|---|---|---|
| 05/06/1974 | ORIG-1 | Approval |
Review (PDF)
|
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/nda/pre96/080816.pdf |
Supplements
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
|---|---|---|---|---|---|
| 12/21/1990 | SUPPL-6 | Labeling |
Label is not available on this site. |
||
| 04/25/1990 | SUPPL-5 | Labeling |
Label is not available on this site. |
||
| 06/17/1991 | SUPPL-4 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 11/26/1986 | SUPPL-3 | Manufacturing (CMC) |
Label is not available on this site. |