phenytoin sodium

Generic: phenytoin sodium

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phenytoin sodium
Generic Name phenytoin sodium
Labeler sun pharmaceutical industries, inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

phenytoin sodium 200 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 62756-299
Product ID 62756-299_c89dfc75-606c-4a4e-9d2b-d907b492a837
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040731
Listing Expiration 2026-12-31
Marketing Start 2008-06-30

Pharmacologic Class

Classes
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]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62756299
Hyphenated Format 62756-299

Supplemental Identifiers

RxCUI
855861 855873
UPC
0362756432833
UNII
4182431BJH

Packaging Origin

Original Packager
true

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 ANDA040731 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-08)
  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-13)
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-83)
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-88)
source: ndc

Packages (4)

62756-299-08 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-08) 62756-299-13 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-13) 62756-299-83 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-83) 62756-299-88 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-88)

Ingredients (1)

phenytoin sodium (200 mg/1)

Linked Drug Pages (1)

phenytoin sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c89dfc75-606c-4a4e-9d2b-d907b492a837", "openfda": {"upc": ["0362756432833"], "unii": ["4182431BJH"], "rxcui": ["855861", "855873"], "spl_set_id": ["c40f66cc-6f4a-4b29-84ba-d265e4848735"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-08)", "package_ndc": "62756-299-08", "marketing_start_date": "20080630"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-13)", "package_ndc": "62756-299-13", "marketing_start_date": "20080630"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-83)", "package_ndc": "62756-299-83", "marketing_start_date": "20080630"}, {"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-88)", "package_ndc": "62756-299-88", "marketing_start_date": "20080630"}], "brand_name": "phenytoin sodium", "product_id": "62756-299_c89dfc75-606c-4a4e-9d2b-d907b492a837", "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": "62756-299", "generic_name": "phenytoin sodium", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "phenytoin sodium", "active_ingredients": [{"name": "PHENYTOIN SODIUM", "strength": "200 mg/1"}], "application_number": "ANDA040731", "marketing_category": "ANDA", "marketing_start_date": "20080630", "listing_expiration_date": "20261231"}