Details for New Drug Application (NDA): 210377
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NDA 210377 describes DIMETHYL FUMARATE, which is a drug marketed by Accord Hlthcare, Alkem Labs Ltd, Amneal, Aurobindo Pharma, Cipla, Glenmark Pharms Ltd, Hetero Labs Ltd Iii, Lupin, Macleods Pharms Ltd, MSN, Mylan, Prinston Inc, Sawai Usa, Sola Pharms, Torrent, Twi Pharms, and Zydus Pharms, and is included in seventeen NDAs. It is available from eighteen suppliers. Additional details are available on the DIMETHYL FUMARATE profile page.
The generic ingredient in DIMETHYL FUMARATE is dimethyl fumarate. There are seventy-six drug master file entries for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the dimethyl fumarate profile page.
The generic ingredient in DIMETHYL FUMARATE is dimethyl fumarate. There are seventy-six drug master file entries for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the dimethyl fumarate profile page.
Summary for 210377
| Tradename: | DIMETHYL FUMARATE |
| Applicant: | Macleods Pharms Ltd |
| Ingredient: | dimethyl fumarate |
| Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 210377
Suppliers and Packaging for NDA: 210377
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| DIMETHYL FUMARATE | dimethyl fumarate | CAPSULE, DELAYED RELEASE;ORAL | 210377 | ANDA | Macleods Pharmaceuticals Limited | 33342-349 | 33342-349-09 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-349-09) |
| DIMETHYL FUMARATE | dimethyl fumarate | CAPSULE, DELAYED RELEASE;ORAL | 210377 | ANDA | Macleods Pharmaceuticals Limited | 33342-349 | 33342-349-94 | 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-349-94) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, DELAYED RELEASE;ORAL | Strength | 120MG | ||||
| Approval Date: | Jun 26, 2024 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, DELAYED RELEASE;ORAL | Strength | 240MG | ||||
| Approval Date: | Jun 26, 2024 | TE: | AB | RLD: | No | ||||
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