phenytoin sodium
Generic: phenytoin sodium
Labeler: aphena pharma solutions - tennessee, llcDrug Facts
Product Profile
Brand Name
phenytoin sodium
Generic Name
phenytoin sodium
Labeler
aphena pharma solutions - tennessee, llc
Dosage Form
CAPSULE, EXTENDED RELEASE
Routes
Active Ingredients
phenytoin sodium 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71610-869
Product ID
71610-869_29b8a9bb-8e99-a599-e063-6394a90ab307
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040684
Listing Expiration
2026-12-31
Marketing Start
2006-09-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71610869
Hyphenated Format
71610-869
Supplemental Identifiers
RxCUI
UNII
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
phenytoin sodium (source: ndc)
Generic Name
phenytoin sodium (source: ndc)
Application Number
ANDA040684 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 270 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71610-869-92)
- 360 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71610-869-94)
- 540 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71610-869-98)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "29b8a9bb-8e99-a599-e063-6394a90ab307", "openfda": {"unii": ["4182431BJH"], "rxcui": ["855671"], "spl_set_id": ["29b8d0a2-a96e-46a5-e063-6394a90a7113"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "270 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71610-869-92)", "package_ndc": "71610-869-92", "marketing_start_date": "20241211"}, {"sample": false, "description": "360 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71610-869-94)", "package_ndc": "71610-869-94", "marketing_start_date": "20241211"}, {"sample": false, "description": "540 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71610-869-98)", "package_ndc": "71610-869-98", "marketing_start_date": "20241211"}], "brand_name": "Phenytoin Sodium", "product_id": "71610-869_29b8a9bb-8e99-a599-e063-6394a90ab307", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Cytochrome P450 1A2 Inducers [MoA]", "Cytochrome P450 2B6 Inducers [MoA]", "Cytochrome P450 2C19 Inducers [MoA]", "Cytochrome P450 2C8 Inducers [MoA]", "Cytochrome P450 2C9 Inducers [MoA]", "Cytochrome P450 2D6 Inducers [MoA]", "Cytochrome P450 3A Inducers [MoA]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71610-869", "generic_name": "Phenytoin Sodium", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenytoin Sodium", "active_ingredients": [{"name": "PHENYTOIN SODIUM", "strength": "100 mg/1"}], "application_number": "ANDA040684", "marketing_category": "ANDA", "marketing_start_date": "20060905", "listing_expiration_date": "20261231"}