Imatinib is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Dr.reddy's Laboratories Inc. The primary component is Imatinib Mesylate.
Product ID | 43598-344_01fcd1cf-5e84-3f2e-d15d-6ba745f4baf9 |
NDC | 43598-344 |
Product Type | Human Prescription Drug |
Proprietary Name | Imatinib |
Generic Name | Imatinib |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2018-08-13 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA206547 |
Labeler Name | Dr.Reddy's Laboratories Inc |
Substance Name | IMATINIB MESYLATE |
Active Ingredient Strength | 100 mg/1 |
Pharm Classes | Kinase Inhibitor [EPC],Protein Kinase Inhibitors [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2018-08-13 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA206547 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-08-13 |
Marketing Category | ANDA |
Application Number | ANDA206547 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-08-13 |
Marketing Category | ANDA |
Application Number | ANDA206547 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2018-08-13 |
Ingredient | Strength |
---|---|
IMATINIB MESYLATE | 100 mg/1 |
SPL SET ID: | 559dd8e5-11f9-70cd-3fb0-9f9eb8484a37 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
43598-344 | Imatinib | Imatinib |
43598-345 | Imatinib | Imatinib |
0378-2245 | Imatinib Mesylate | imatinib |
0378-2246 | Imatinib Mesylate | imatinib |
42292-043 | Imatinib Mesylate | imatinib |
42292-044 | Imatinib Mesylate | imatinib |
51407-269 | Imatinib Mesylate | imatinib |
51407-270 | Imatinib Mesylate | imatinib |
65162-794 | Imatinib Mesylate | Imatinib |
65162-795 | Imatinib Mesylate | Imatinib |
68180-390 | IMATINIB MESYLATE | IMATINIB |