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NDC 00378-0636-91 Iloperidone 12 mg/1 Details
Iloperidone 12 mg/1
Iloperidone is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Mylan Pharmaceuticals Inc.. The primary component is ILOPERIDONE.
MedlinePlus Drug Summary
Iloperidone is used to treat the symptoms of schizophrenia (a mental illness that causes disturbed or unusual thinking, loss of interest in life, and strong or inappropriate emotions). Iloperidone is in a class of medications called atypical antipsychotics. It works by changing the activity of certain natural substances in the brain.
Related Packages: 00378-0636-91Last Updated: 02/05/2023
MedLinePlus Full Drug Details: Iloperidone
Product Information
| NDC | 00378-0636 |
|---|---|
| Product ID | 0378-0636_dcf849c7-acfc-4b32-ab2e-2e3d30c636f2 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Iloperidone |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Iloperidone |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 12 |
| Active Ingredient Units | mg/1 |
| Substance Name | ILOPERIDONE |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Pharmaceutical Class | Atypical Antipsychotic [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA207231 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00378-0636-91 (00378063691)
| NDC Package Code | 0378-0636-91 |
|---|---|
| Billing NDC | 00378063691 |
| Package | 60 TABLET in 1 BOTTLE (0378-0636-91) |
| Marketing Start Date | 2017-03-20 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |