chloramphenicol sodium succinate
Generic: chloramphenicol sodium succinate
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
chloramphenicol sodium succinate
Generic Name
chloramphenicol sodium succinate
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
chloramphenicol sodium succinate 1 g/10mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-011
Product ID
63323-011_f0af962d-5024-47cf-b7a0-da9b5ff3c994
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062365
Listing Expiration
2026-12-31
Marketing Start
2001-01-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323011
Hyphenated Format
63323-011
Supplemental Identifiers
RxCUI
UNII
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
chloramphenicol sodium succinate (source: ndc)
Generic Name
chloramphenicol sodium succinate (source: ndc)
Application Number
ANDA062365 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/10mL
Packaging
- 10 VIAL in 1 TRAY (63323-011-15) / 10 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f0af962d-5024-47cf-b7a0-da9b5ff3c994", "openfda": {"unii": ["872109HX6B"], "rxcui": ["239200"], "spl_set_id": ["aed29594-211d-49ef-813f-131975a8d0e3"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 TRAY (63323-011-15) / 10 mL in 1 VIAL", "package_ndc": "63323-011-15", "marketing_start_date": "20010112"}], "brand_name": "Chloramphenicol Sodium Succinate", "product_id": "63323-011_f0af962d-5024-47cf-b7a0-da9b5ff3c994", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Amphenicol-class Antibacterial [EPC]", "Amphenicols [EXT]"], "product_ndc": "63323-011", "generic_name": "CHLORAMPHENICOL SODIUM SUCCINATE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chloramphenicol Sodium Succinate", "active_ingredients": [{"name": "CHLORAMPHENICOL SODIUM SUCCINATE", "strength": "1 g/10mL"}], "application_number": "ANDA062365", "marketing_category": "ANDA", "marketing_start_date": "20010112", "listing_expiration_date": "20261231"}