Details for New Drug Application (NDA): 206484
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The generic ingredient in HYDROCODONE BITARTRATE AND ACETAMINOPHEN is acetaminophen; hydrocodone bitartrate. There are sixty-six drug master file entries for this compound. Thirty-eight suppliers are listed for this compound. Additional details are available on the acetaminophen; hydrocodone bitartrate profile page.
Summary for 206484
Tradename: | HYDROCODONE BITARTRATE AND ACETAMINOPHEN |
Applicant: | Upsher Smith Labs |
Ingredient: | acetaminophen; hydrocodone bitartrate |
Patents: | 0 |
Pharmacology for NDA: 206484
Mechanism of Action | Opioid Agonists |
Suppliers and Packaging for NDA: 206484
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
HYDROCODONE BITARTRATE AND ACETAMINOPHEN | acetaminophen; hydrocodone bitartrate | TABLET;ORAL | 206484 | ANDA | Upsher-Smith Laboratories, LLC | 0245-0410 | 0245-0410-01 | 100 BLISTER PACK in 1 CARTON (0245-0410-01) / 1 TABLET in 1 BLISTER PACK (0245-0410-89) |
HYDROCODONE BITARTRATE AND ACETAMINOPHEN | acetaminophen; hydrocodone bitartrate | TABLET;ORAL | 206484 | ANDA | Upsher-Smith Laboratories, LLC | 0245-0410 | 0245-0410-11 | 100 TABLET in 1 BOTTLE (0245-0410-11) |
Profile for product number 001
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 325MG;5MG | ||||
Approval Date: | Mar 24, 2017 | TE: | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 325MG;7.5MG | ||||
Approval Date: | Mar 24, 2017 | TE: | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 325MG;10MG | ||||
Approval Date: | Mar 24, 2017 | TE: | RLD: | No |
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