sezaby
Generic: phenobarbital sodium
Labeler: sun pharmaceutical industries, inc.Drug Facts
Product Profile
Brand Name
sezaby
Generic Name
phenobarbital sodium
Labeler
sun pharmaceutical industries, inc.
Dosage Form
INJECTION
Routes
Active Ingredients
phenobarbital sodium 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62756-301
Product ID
62756-301_842763a1-63ca-4721-b127-f997ac4aa659
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA215910
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2022-12-25
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62756301
Hyphenated Format
62756-301
Supplemental Identifiers
RxCUI
UPC
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
sezaby (source: ndc)
Generic Name
phenobarbital sodium (source: ndc)
Application Number
NDA215910 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 1 INJECTION in 1 VIAL, SINGLE-DOSE (62756-301-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "842763a1-63ca-4721-b127-f997ac4aa659", "openfda": {"upc": ["0362756301016"], "unii": ["SW9M9BB5K3"], "rxcui": ["2624719", "2624724"], "spl_set_id": ["8c7d0402-4977-4c25-bc4b-11db91339e9a"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION in 1 VIAL, SINGLE-DOSE (62756-301-01)", "package_ndc": "62756-301-01", "marketing_start_date": "20221226"}], "brand_name": "SEZABY", "product_id": "62756-301_842763a1-63ca-4721-b127-f997ac4aa659", "dosage_form": "INJECTION", "product_ndc": "62756-301", "dea_schedule": "CIV", "generic_name": "phenobarbital sodium", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SEZABY", "active_ingredients": [{"name": "PHENOBARBITAL SODIUM", "strength": "100 mg/1"}], "application_number": "NDA215910", "marketing_category": "NDA", "marketing_start_date": "20221225", "listing_expiration_date": "20261231"}