Details for New Drug Application (NDA): 209993
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The generic ingredient in METFORMIN HYDROCHLORIDE is metformin hydrochloride; saxagliptin hydrochloride. There are forty-nine drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the metformin hydrochloride; saxagliptin hydrochloride profile page.
Summary for 209993
Tradename: | METFORMIN HYDROCHLORIDE |
Applicant: | Qingdao Baheal Pharm |
Ingredient: | metformin hydrochloride |
Patents: | 0 |
Suppliers and Packaging for NDA: 209993
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 209993 | ANDA | EPIC PHARMA, LLC | 42806-405 | 42806-405-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-405-60) |
METFORMIN HYDROCHLORIDE | metformin hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 209993 | ANDA | EPIC PHARMA, LLC | 42806-406 | 42806-406-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-406-60) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 500MG | ||||
Approval Date: | Dec 27, 2018 | TE: | AB2 | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 1GM | ||||
Approval Date: | Dec 27, 2018 | TE: | AB2 | RLD: | No |
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