Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 210356
Company: FRESENIUS KABI USA
Company: FRESENIUS KABI USA
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
HALOPERIDOL | HALOPERIDOL LACTATE | EQ 5MG BASE/ML | INJECTABLE;INJECTION | Prescription | AP | 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 |
---|---|---|---|---|---|---|---|
07/01/2019 | ORIG-1 | Approval | STANDARD |
Label is not available on this site. |
Supplements
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
---|---|---|---|---|---|
06/27/2023 | SUPPL-2 | Labeling-Package Insert |
Label is not available on this site. |
HALOPERIDOL
INJECTABLE;INJECTION; EQ 5MG BASE/ML
TE Code = AP
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company |
---|---|---|---|---|---|---|---|---|
HALOPERIDOL | HALOPERIDOL LACTATE | EQ 5MG BASE/ML | INJECTABLE;INJECTION | Prescription | No | AP | 075689 | FRESENIUS KABI USA |
HALOPERIDOL | HALOPERIDOL LACTATE | EQ 5MG BASE/ML | INJECTABLE;INJECTION | Prescription | No | AP | 210356 | FRESENIUS KABI USA |
HALOPERIDOL | HALOPERIDOL LACTATE | EQ 5MG BASE/ML | INJECTABLE;INJECTION | Prescription | No | AP | 076774 | GLAND PHARMA LTD |
HALOPERIDOL | HALOPERIDOL LACTATE | EQ 5MG BASE/ML | INJECTABLE;INJECTION | Prescription | No | AP | 075858 | HIKMA |
HALOPERIDOL | HALOPERIDOL LACTATE | EQ 5MG BASE/ML | INJECTABLE;INJECTION | Prescription | No | AP | 078347 | MYLAN LABS LTD |
HALOPERIDOL | HALOPERIDOL LACTATE | EQ 5MG BASE/ML | INJECTABLE;INJECTION | Prescription | No | AP | 091637 | SAGENT PHARMS |
HALOPERIDOL | HALOPERIDOL LACTATE | EQ 5MG BASE/ML | INJECTABLE;INJECTION | Prescription | No | AP | 200742 | SAGENT PHARMS |