Details for New Drug Application (NDA): 040103
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NDA 040103 describes BENZTROPINE MESYLATE, which is a drug marketed by Fresenius Kabi Usa, Hikma, Hikma Farmaceutica, Luitpold, Navinta Llc, Aiping Pharm Inc, Chartwell Rx, Epic Pharma Llc, Invagen Pharms, Lannett Co Inc, Leading, Nuvo Pharm, Oxford Pharms, Ph Health, Pliva, Quagen, Quantum Pharmics, and Usl Pharma, and is included in twenty-eight NDAs. It is available from twenty-one suppliers. Additional details are available on the BENZTROPINE MESYLATE profile page.
The generic ingredient in BENZTROPINE MESYLATE is benztropine mesylate. There are seven drug master file entries for this compound. Twenty-one suppliers are listed for this compound. Additional details are available on the benztropine mesylate profile page.
The generic ingredient in BENZTROPINE MESYLATE is benztropine mesylate. There are seven drug master file entries for this compound. Twenty-one suppliers are listed for this compound. Additional details are available on the benztropine mesylate profile page.
Summary for 040103
| Tradename: | BENZTROPINE MESYLATE |
| Applicant: | Aiping Pharm Inc |
| Ingredient: | benztropine mesylate |
| Patents: | 0 |
Pharmacology for NDA: 040103
| Mechanism of Action | Cholinergic Antagonists Histamine Receptor Antagonists |
Medical Subject Heading (MeSH) Categories for 040103
Suppliers and Packaging for NDA: 040103
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| BENZTROPINE MESYLATE | benztropine mesylate | TABLET;ORAL | 040103 | ANDA | ScieGen Pharmaceuticals Inc | 50228-225 | 50228-225-01 | 100 TABLET in 1 BOTTLE (50228-225-01) |
| BENZTROPINE MESYLATE | benztropine mesylate | TABLET;ORAL | 040103 | ANDA | ScieGen Pharmaceuticals Inc | 50228-225 | 50228-225-10 | 1000 TABLET in 1 BOTTLE (50228-225-10) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 0.5MG | ||||
| Approval Date: | Dec 12, 1996 | TE: | AA | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 1MG | ||||
| Approval Date: | Dec 12, 1996 | TE: | AA | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 2MG | ||||
| Approval Date: | Dec 12, 1996 | TE: | AA | RLD: | No | ||||
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