Oxytocin is a Intramuscular; Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Fresenius Kabi Usa, Llc. The primary component is Oxytocin.
Product ID | 63323-012_1ea6fccc-d789-4560-a50e-a89f2126d7e5 |
NDC | 63323-012 |
Product Type | Human Prescription Drug |
Proprietary Name | Oxytocin |
Generic Name | Oxytocin |
Dosage Form | Injection, Solution |
Route of Administration | INTRAMUSCULAR; INTRAVENOUS |
Marketing Start Date | 2000-08-10 |
Marketing Category | NDA / NDA |
Application Number | NDA018248 |
Labeler Name | Fresenius Kabi USA, LLC |
Substance Name | OXYTOCIN |
Active Ingredient Strength | 10 [USP'U]/mL |
Pharm Classes | Increased Uterine Smooth Muscle Contraction or Tone [PE],Oxytocic [EPC],Oxytocin [CS] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2019-11-08 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA018248 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2000-08-10 |
Marketing Category | NDA |
Application Number | NDA018248 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2019-06-14 |
Marketing Category | NDA |
Application Number | NDA018248 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2019-06-14 |
Marketing Category | NDA |
Application Number | NDA018248 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-06-14 |
Marketing Category | NDA |
Application Number | NDA018248 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2000-08-10 |
Marketing Category | NDA |
Application Number | NDA018248 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2000-08-10 |
Marketing Category | NDA |
Application Number | NDA018248 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2020-02-05 |
Marketing Category | NDA |
Application Number | NDA018248 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2000-08-10 |
Marketing Category | NDA |
Application Number | NDA018248 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2020-03-04 |
Marketing Category | NDA |
Application Number | NDA018248 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2019-11-08 |
Marketing Category | NDA |
Application Number | NDA018248 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-06-14 |
Marketing Category | NDA |
Application Number | NDA018248 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2000-08-10 |
Ingredient | Strength |
---|---|
OXYTOCIN | 10 [USP'U]/mL |
SPL SET ID: | 6d7d1280-f286-4f39-89f3-2b96571810e6 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
0143-9742 | Oxytocin | Oxytocin |
0143-9743 | Oxytocin | Oxytocin |
0641-6114 | Oxytocin | Oxytocin |
0641-6115 | Oxytocin | Oxytocin |
52533-048 | Oxytocin | Oxytocin |
52533-051 | Oxytocin | Oxytocin |
52533-054 | Oxytocin | Oxytocin |
52533-055 | Oxytocin | Oxytocin |
52533-056 | Oxytocin | Oxytocin |
52533-105 | Oxytocin | Oxytocin |
52533-170 | Oxytocin | Oxytocin |
52533-233 | Oxytocin | Oxytocin |
52533-234 | Oxytocin | Oxytocin |
55154-9356 | Oxytocin | OXYTOCIN |
55154-9577 | Oxytocin | OXYTOCIN |
55154-9584 | Oxytocin | OXYTOCIN |
63323-012 | Oxytocin | OXYTOCIN |
42023-116 | Pitocin | oxytocin |
42023-130 | Pitocin | oxytocin |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
OXYTOCIN 78368996 not registered Dead/Abandoned |
Hirsch, Eric Michael 2004-02-17 |