ARTICAINE is a Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Ndc, Inc.. The primary component is Articaine Hydro.
Product ID | 43128-101_10cad14a-4cb4-4fbb-96cc-cda1dfca2a53 |
NDC | 43128-101 |
Product Type | Human Prescription Drug |
Proprietary Name | ARTICAINE |
Generic Name | Articaine Hydrochloride And Epinephrine |
Dosage Form | Injection, Solution |
Route of Administration | SUBCUTANEOUS |
Marketing Start Date | 2015-06-22 |
Marketing Category | NDA / NDA |
Application Number | NDA020971 |
Labeler Name | NDC, Inc. |
Substance Name | ARTICAINE HYDRO |
Active Ingredient Strength | 40 mg/mL; mg/mL |
Pharm Classes | Amide Local Ane |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2015-06-22 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA020971 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-06-22 |
Ingredient | Strength |
---|---|
ARTICAINE HYDROCHLORIDE | 40 mg/mL |
SPL SET ID: | 0b0cbbec-8216-434f-892e-226c89d7239c |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
43128-101 | ARTICAINE | Articaine Hydrochloride and Epinephrine |
43128-102 | ARTICAINE | Articaine Hydrochloride and Epinephrine |
50227-1040 | ARTICAINE | Articaine Hydrochloride and Epinephrine |
50227-1050 | ARTICAINE | Articaine Hydrochloride and Epinephrine |
66975-417 | ARTICAINE | Articaine Hydrochloride and Epinephrine |
66975-418 | ARTICAINE | Articaine Hydrochloride and Epinephrine |
0404-6620 | Articaine Hydrochloride and Epinephrine | Articaine Hydrochloride and Epinephrine |
0404-6625 | Articaine Hydrochloride and Epinephrine | Articaine Hydrochloride and Epinephrine |
0362-0830 | Zorcaine | Articaine Hydrochloride and Epinephrine |