Details for New Drug Application (NDA): 210758
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The generic ingredient in OXYCODONE HYDROCHLORIDE is ibuprofen; oxycodone hydrochloride. There are sixty-four drug master file entries for this compound. Additional details are available on the ibuprofen; oxycodone hydrochloride profile page.
Summary for 210758
Tradename: | OXYCODONE HYDROCHLORIDE |
Applicant: | Specgx Llc |
Ingredient: | oxycodone hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 210758
Mechanism of Action | Full Opioid Agonists |
Suppliers and Packaging for NDA: 210758
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
OXYCODONE HYDROCHLORIDE | oxycodone hydrochloride | SOLUTION;ORAL | 210758 | ANDA | SpecGx LLC | 0406-8556 | 0406-8556-05 | 1 BOTTLE, PLASTIC in 1 CARTON (0406-8556-05) / 500 mL in 1 BOTTLE, PLASTIC |
OXYCODONE HYDROCHLORIDE | oxycodone hydrochloride | SOLUTION;ORAL | 210758 | ANDA | SpecGx LLC | 0406-8557 | 0406-8557-30 | 1 BOTTLE, PLASTIC in 1 CARTON (0406-8557-30) / 30 mL in 1 BOTTLE, PLASTIC |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;ORAL | Strength | 5MG/5ML | ||||
Approval Date: | Apr 30, 2018 | TE: | AA | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;ORAL | Strength | 100MG/5ML | ||||
Approval Date: | Apr 30, 2018 | TE: | AA | RLD: | No |
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