Details for New Drug Application (NDA): 207176
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The generic ingredient in HOMATROPINE METHYLBROMIDE AND HYDROCODONE BITARTRATE is homatropine methylbromide; hydrocodone bitartrate. There are five drug master file entries for this compound. Six suppliers are listed for this compound. Additional details are available on the homatropine methylbromide; hydrocodone bitartrate profile page.
Summary for 207176
| Tradename: | HOMATROPINE METHYLBROMIDE AND HYDROCODONE BITARTRATE |
| Applicant: | Avanthi Inc |
| Ingredient: | homatropine methylbromide; hydrocodone bitartrate |
| Patents: | 0 |
Pharmacology for NDA: 207176
| Mechanism of Action | Opioid Agonists |
Suppliers and Packaging for NDA: 207176
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| HOMATROPINE METHYLBROMIDE AND HYDROCODONE BITARTRATE | homatropine methylbromide; hydrocodone bitartrate | TABLET;ORAL | 207176 | ANDA | KVK-Tech, Inc. | 10702-055 | 10702-055-01 | 100 TABLET in 1 BOTTLE (10702-055-01) |
| HOMATROPINE METHYLBROMIDE AND HYDROCODONE BITARTRATE | homatropine methylbromide; hydrocodone bitartrate | TABLET;ORAL | 207176 | ANDA | KVK-Tech, Inc. | 10702-055 | 10702-055-03 | 30 TABLET in 1 BOTTLE (10702-055-03) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 1.5MG;5MG | ||||
| Approval Date: | Aug 7, 2017 | TE: | AA | RLD: | No | ||||
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