Details for New Drug Application (NDA): 217269
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NDA 217269 describes GUANFACINE HYDROCHLORIDE, which is a drug marketed by Actavis Elizabeth, Alembic, Apotex, Fosun Wanbang, Impax Labs Inc, Pharmobedient, Rubicon Research, Sandoz, Sun Pharm, Teva Pharms Usa, Twi Pharms, Unichem, Yichang Humanwell, Aiping Pharm Inc, Ajanta Pharma Ltd, Amneal Pharm, Aurobindo Pharma Usa, Epic Pharma Llc, I 3 Pharms, Watson Labs, and Xiromed, and is included in twenty-four NDAs. It is available from thirty-seven suppliers. Additional details are available on the GUANFACINE HYDROCHLORIDE profile page.
The generic ingredient in GUANFACINE HYDROCHLORIDE is guanfacine hydrochloride. There are seven drug master file entries for this compound. Thirty-eight suppliers are listed for this compound. Additional details are available on the guanfacine hydrochloride profile page.
The generic ingredient in GUANFACINE HYDROCHLORIDE is guanfacine hydrochloride. There are seven drug master file entries for this compound. Thirty-eight suppliers are listed for this compound. Additional details are available on the guanfacine hydrochloride profile page.
Summary for 217269
| Tradename: | GUANFACINE HYDROCHLORIDE |
| Applicant: | Alembic |
| Ingredient: | guanfacine hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 217269
| Mechanism of Action | Adrenergic alpha2-Agonists |
Medical Subject Heading (MeSH) Categories for 217269
Suppliers and Packaging for NDA: 217269
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| GUANFACINE HYDROCHLORIDE | guanfacine hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 217269 | ANDA | Alembic Pharmaceuticals Limited | 46708-745 | 46708-745-31 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-745-31) |
| GUANFACINE HYDROCHLORIDE | guanfacine hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 217269 | ANDA | Alembic Pharmaceuticals Limited | 46708-745 | 46708-745-91 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-745-91) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | EQ 1MG BASE | ||||
| Approval Date: | Aug 7, 2023 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | EQ 2MG BASE | ||||
| Approval Date: | Aug 7, 2023 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | EQ 3MG BASE | ||||
| Approval Date: | Aug 7, 2023 | TE: | AB | RLD: | No | ||||
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