Details for New Drug Application (NDA): 213219
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The generic ingredient in CLOMIPRAMINE HYDROCHLORIDE is clomipramine hydrochloride. There are eleven drug master file entries for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the clomipramine hydrochloride profile page.
Summary for 213219
| Tradename: | CLOMIPRAMINE HYDROCHLORIDE |
| Applicant: | Micro Labs |
| Ingredient: | clomipramine hydrochloride |
| Patents: | 0 |
Suppliers and Packaging for NDA: 213219
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| CLOMIPRAMINE HYDROCHLORIDE | clomipramine hydrochloride | CAPSULE;ORAL | 213219 | ANDA | Micro Labs Limited | 42571-342 | 42571-342-01 | 100 CAPSULE in 1 BOTTLE (42571-342-01) |
| CLOMIPRAMINE HYDROCHLORIDE | clomipramine hydrochloride | CAPSULE;ORAL | 213219 | ANDA | Micro Labs Limited | 42571-342 | 42571-342-05 | 500 CAPSULE in 1 BOTTLE (42571-342-05) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 25MG | ||||
| Approval Date: | Jun 22, 2020 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 50MG | ||||
| Approval Date: | Jun 22, 2020 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 75MG | ||||
| Approval Date: | Jun 22, 2020 | TE: | AB | RLD: | No | ||||
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