Details for New Drug Application (NDA): 076934
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NDA 076934 describes SERTRALINE HYDROCHLORIDE, which is a drug marketed by Almatica, Aurobindo Pharma, Ranbaxy Labs Ltd, Strides Pharma, Accord Hlthcare, Anda Repository, Appco, Ascent Pharms Inc, Chartwell Molecular, Granules, Heritage Pharma Avet, Hikma Pharms, Invagen Pharms, Ivax Sub Teva Pharms, Lupin, Mylan Pharms Inc, Norvium Bioscience, Oxford Pharms, Reyoung, Sciegen Pharms Inc, Sun Pharm Inds (in), Sun Pharm Inds Ltd, Torrent Pharms, Viwit Pharm, and Zydus, and is included in thirty-one NDAs. It is available from forty-five suppliers. Additional details are available on the SERTRALINE HYDROCHLORIDE profile page.
The generic ingredient in SERTRALINE HYDROCHLORIDE is sertraline hydrochloride. There are twenty-two drug master file entries for this compound. Forty-eight suppliers are listed for this compound. Additional details are available on the sertraline hydrochloride profile page.
The generic ingredient in SERTRALINE HYDROCHLORIDE is sertraline hydrochloride. There are twenty-two drug master file entries for this compound. Forty-eight suppliers are listed for this compound. Additional details are available on the sertraline hydrochloride profile page.
Summary for 076934
| Tradename: | SERTRALINE HYDROCHLORIDE |
| Applicant: | Strides Pharma |
| Ingredient: | sertraline hydrochloride |
| Patents: | 0 |
Pharmacology for NDA: 076934
| Mechanism of Action | Cytochrome P450 2D6 Inhibitors Serotonin Uptake Inhibitors |
Medical Subject Heading (MeSH) Categories for 076934
Suppliers and Packaging for NDA: 076934
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| SERTRALINE HYDROCHLORIDE | sertraline hydrochloride | CONCENTRATE;ORAL | 076934 | ANDA | Bryant Ranch Prepack | 63629-8774 | 63629-8774-1 | 1 BOTTLE, DROPPER in 1 CARTON (63629-8774-1) / 60 mL in 1 BOTTLE, DROPPER |
| SERTRALINE HYDROCHLORIDE | sertraline hydrochloride | CONCENTRATE;ORAL | 076934 | ANDA | ACI Healthcare USA, Inc. | 71093-143 | 71093-143-11 | 1 BOTTLE, DROPPER in 1 CARTON (71093-143-11) / 60 mL in 1 BOTTLE, DROPPER |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CONCENTRATE;ORAL | Strength | EQ 20MG BASE/ML | ||||
| Approval Date: | Jun 30, 2006 | TE: | AA | RLD: | No | ||||
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