Details for New Drug Application (NDA): 214255
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NDA 214255 describes VARENICLINE TARTRATE, which is a drug marketed by Ajanta Pharma Ltd, Alkem Labs Ltd, Apotex, Avalanche Pharm, Dr Reddys, Endo Operations, Hetero Labs Ltd Iii, Leading Pharma, Lupin Ltd, Mankind Pharma, Mylan, Piramal, and Zydus, and is included in thirteen NDAs. It is available from twenty suppliers. Additional details are available on the VARENICLINE TARTRATE profile page.
The generic ingredient in VARENICLINE TARTRATE is varenicline tartrate. There are twelve drug master file entries for this compound. Twenty-four suppliers are listed for this compound. Additional details are available on the varenicline tartrate profile page.
The generic ingredient in VARENICLINE TARTRATE is varenicline tartrate. There are twelve drug master file entries for this compound. Twenty-four suppliers are listed for this compound. Additional details are available on the varenicline tartrate profile page.
Summary for 214255
| Tradename: | VARENICLINE TARTRATE |
| Applicant: | Mankind Pharma |
| Ingredient: | varenicline tartrate |
| Patents: | 0 |
Pharmacology for NDA: 214255
| Mechanism of Action | Cholinergic Agonists Partial Cholinergic Nicotinic Agonists |
Medical Subject Heading (MeSH) Categories for 214255
Suppliers and Packaging for NDA: 214255
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| VARENICLINE TARTRATE | varenicline tartrate | TABLET;ORAL | 214255 | ANDA | Glenmark Pharmaceuticals Inc., USA | 68462-893 | 68462-893-56 | 56 TABLET, FILM COATED in 1 BOTTLE (68462-893-56) |
| VARENICLINE TARTRATE | varenicline tartrate | TABLET;ORAL | 214255 | ANDA | Glenmark Pharmaceuticals Inc., USA | 68462-894 | 68462-894-04 | 1 BLISTER PACK in 1 CARTON (68462-894-04) / 56 TABLET, FILM COATED in 1 BLISTER PACK |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 0.5MG BASE | ||||
| Approval Date: | Aug 1, 2023 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 1MG BASE | ||||
| Approval Date: | Aug 1, 2023 | TE: | AB | RLD: | No | ||||
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