oxytocin
Generic: oxytocin
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
oxytocin
Generic Name
oxytocin
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
oxytocin 10 [USP'U]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-012
Product ID
63323-012_3649e8ed-929c-4600-9d63-3d77fbe3a0f5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA018248
Listing Expiration
2027-12-31
Marketing Start
2000-08-10
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323012
Hyphenated Format
63323-012
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
oxytocin (source: ndc)
Generic Name
oxytocin (source: ndc)
Application Number
NDA018248 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 [USP'U]/mL
Packaging
- 25 VIAL, MULTI-DOSE in 1 TRAY (63323-012-10) / 10 mL in 1 VIAL, MULTI-DOSE (63323-012-06)
- 25 VIAL in 1 TRAY (63323-012-11) / 1 mL in 1 VIAL (63323-012-03)
- 10 VIAL, MULTI-DOSE in 1 TRAY (63323-012-30) / 30 mL in 1 VIAL, MULTI-DOSE (63323-012-02)
Packages (3)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "3649e8ed-929c-4600-9d63-3d77fbe3a0f5", "openfda": {"nui": ["N0000009705", "N0000175828", "M0015703"], "upc": ["0363323012069", "0363323012038", "0363323012021"], "unii": ["1JQS135EYN"], "rxcui": ["238013", "1791721"], "spl_set_id": ["c7fd585a-99b7-4309-b003-a6cbef05372c"], "pharm_class_cs": ["Oxytocin [CS]"], "pharm_class_pe": ["Increased Uterine Smooth Muscle Contraction or Tone [PE]"], "pharm_class_epc": ["Oxytocic [EPC]"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 TRAY (63323-012-10) / 10 mL in 1 VIAL, MULTI-DOSE (63323-012-06)", "package_ndc": "63323-012-10", "marketing_start_date": "20000810"}, {"sample": false, "description": "25 VIAL in 1 TRAY (63323-012-11) / 1 mL in 1 VIAL (63323-012-03)", "package_ndc": "63323-012-11", "marketing_start_date": "20000810"}, {"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 TRAY (63323-012-30) / 30 mL in 1 VIAL, MULTI-DOSE (63323-012-02)", "package_ndc": "63323-012-30", "marketing_start_date": "20000810"}], "brand_name": "Oxytocin", "product_id": "63323-012_3649e8ed-929c-4600-9d63-3d77fbe3a0f5", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Uterine Smooth Muscle Contraction or Tone [PE]", "Oxytocic [EPC]", "Oxytocin [CS]"], "product_ndc": "63323-012", "generic_name": "OXYTOCIN", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxytocin", "active_ingredients": [{"name": "OXYTOCIN", "strength": "10 [USP'U]/mL"}], "application_number": "NDA018248", "marketing_category": "NDA", "marketing_start_date": "20000810", "listing_expiration_date": "20271231"}