Details for New Drug Application (NDA): 217411
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The generic ingredient in AMITRIPTYLINE HYDROCHLORIDE is amitriptyline hydrochloride. There are thirteen drug master file entries for this compound. Thirty-three suppliers are listed for this compound. Additional details are available on the amitriptyline hydrochloride profile page.
Summary for 217411
| Tradename: | AMITRIPTYLINE HYDROCHLORIDE |
| Applicant: | Rising |
| Ingredient: | amitriptyline hydrochloride |
| Patents: | 0 |
Suppliers and Packaging for NDA: 217411
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| AMITRIPTYLINE HYDROCHLORIDE | amitriptyline hydrochloride | TABLET;ORAL | 217411 | ANDA | Major Pharmaceuticals | 0904-7410 | 0904-7410-61 | 100 BLISTER PACK in 1 CARTON (0904-7410-61) / 1 TABLET in 1 BLISTER PACK |
| AMITRIPTYLINE HYDROCHLORIDE | amitriptyline hydrochloride | TABLET;ORAL | 217411 | ANDA | Major Pharmaceuticals | 0904-7411 | 0904-7411-61 | 100 BLISTER PACK in 1 CARTON (0904-7411-61) / 1 TABLET in 1 BLISTER PACK |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
| Approval Date: | May 19, 2023 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 25MG | ||||
| Approval Date: | May 19, 2023 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 50MG | ||||
| Approval Date: | May 19, 2023 | TE: | AB | RLD: | No | ||||
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