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NDC 00362-0830-05 Zorcaine 40; .01 mg/mL; mg/mL Details
Zorcaine 40; .01 mg/mL; mg/mL
Zorcaine is a SUBCUTANEOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Septodont, Inc.. The primary component is ARTICAINE HYDROCHLORIDE; EPINEPHRINE BITARTRATE.
Product Information
NDC | 00362-0830 |
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Product ID | 0362-0830_9c472db9-adc1-414b-8388-95f602c7a901 |
Associated GPIs | |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Zorcaine |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Articaine Hydrochloride and Epinephrine |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | INJECTION, SOLUTION |
Route | SUBCUTANEOUS |
Active Ingredient Strength | 40; .01 |
Active Ingredient Units | mg/mL; mg/mL |
Substance Name | ARTICAINE HYDROCHLORIDE; EPINEPHRINE BITARTRATE |
Labeler Name | Septodont, Inc. |
Pharmaceutical Class | Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Amide Local Anesthetic [EPC], Amides [CS], Catecholamine [EPC], Catecholamines [CS], Local Anesthesia [PE], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC] |
DEA Schedule | n/a |
Marketing Category | NDA AUTHORIZED GENERIC |
Application Number | NDA020971 |
Listing Certified Through | 2024-12-31 |
Package
NDC 00362-0830-05 (00362083005)
NDC Package Code | 0362-0830-05 |
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Billing NDC | 00362083005 |
Package | 50 CARTRIDGE in 1 CARTON (0362-0830-05) / 1.7 mL in 1 CARTRIDGE |
Marketing Start Date | 2019-04-05 |
NDC Exclude Flag | N |
Pricing Information | N/A |