Cefotaxime is a Intramuscular; Intravenous Powder, For Solution in the Human Prescription Drug category. It is labeled and distributed by Sterimax Inc.. The primary component is Cefotaxime Sodium.
Product ID | 21586-012_35c9bd8d-503c-4ac8-aeec-52c3cb708782 |
NDC | 21586-012 |
Product Type | Human Prescription Drug |
Proprietary Name | Cefotaxime |
Generic Name | Cefotaxime Injection |
Dosage Form | Powder, For Solution |
Route of Administration | INTRAMUSCULAR; INTRAVENOUS |
Marketing Start Date | 2019-08-01 |
Marketing Category | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE / UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
Labeler Name | SteriMax Inc. |
Substance Name | CEFOTAXIME 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 | 2019-08-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | Unapproved drug for use in drug shor |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-08-01 |
Marketing Category | Unapproved drug for use in drug shor |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-08-01 |
Ingredient | Strength |
---|---|
CEFOTAXIME SODIUM | 2 g/1 |
SPL SET ID: | 8efe3bd0-c43a-2bd6-e053-2a95a90a92fa |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0143-9930 | Cefotaxime | Cefotaxime |
0143-9931 | Cefotaxime | Cefotaxime |
0143-9933 | Cefotaxime | Cefotaxime |
0143-9935 | Cefotaxime | Cefotaxime |
21586-011 | Cefotaxime | cefotaxime injection |
21586-012 | Cefotaxime | cefotaxime injection |
55648-947 | CEFOTAXIME | CEFOTAXIME |
55648-948 | CEFOTAXIME | CEFOTAXIME |
55648-986 | CEFOTAXIME | CEFOTAXIME |
64679-947 | Cefotaxime | Cefotaxime |
64679-948 | Cefotaxime | Cefotaxime |
64679-986 | Cefotaxime | Cefotaxime |
68180-811 | CEFOTAXIME | CEFOTAXIME |
68180-822 | CEFOTAXIME | CEFOTAXIME |
68180-833 | CEFOTAXIME | CEFOTAXIME |