Cefoxitin is a Intravenous Injection, Powder, For Solution in the Human Prescription Drug category. It is labeled and distributed by Wg Critical Care, Llc. The primary component is Cefoxitin Sodium.
Product ID | 44567-246_26bbc0f0-42bd-41d1-807e-d76c450a01cb |
NDC | 44567-246 |
Product Type | Human Prescription Drug |
Proprietary Name | Cefoxitin |
Generic Name | Cefoxitin |
Dosage Form | Injection, Powder, For Solution |
Route of Administration | INTRAVENOUS |
Marketing Start Date | 2015-02-18 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA065414 |
Labeler Name | WG Critical Care, LLC |
Substance Name | CEFOXITIN SODIUM |
Active Ingredient Strength | 2 g/1 |
Pharm Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [CS] |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |
Marketing Start Date | 2015-02-18 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA065414 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-02-18 |
Marketing Category | ANDA |
Application Number | ANDA065414 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2017-07-10 |
Ingredient | Strength |
---|---|
CEFOXITIN SODIUM | 2 g/1 |
SPL SET ID: | 91ac4c14-8dd8-4efe-a462-d1c488a6184f |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0143-9876 | Cefoxitin | Cefoxitin |
0143-9877 | Cefoxitin | Cefoxitin |
0143-9878 | Cefoxitin | Cefoxitin |
25021-109 | Cefoxitin | cefoxitin |
25021-110 | Cefoxitin | cefoxitin |
25021-111 | Cefoxitin | cefoxitin |
44567-245 | Cefoxitin | Cefoxitin |
44567-246 | Cefoxitin | Cefoxitin |
44567-247 | Cefoxitin | Cefoxitin |
60505-0759 | Cefoxitin | CEFOXITIN |
60505-0760 | Cefoxitin | CEFOXITIN |
60505-0761 | Cefoxitin | CEFOXITIN |
63323-341 | Cefoxitin | Cefoxitin Sodium |
63323-342 | Cefoxitin | Cefoxitin Sodium |
63323-343 | Cefoxitin | Cefoxitin |
66288-4100 | Cefoxitin | Cefoxitin |