lamotrigine

Generic: lamotrigine

Labeler: dr.reddy's laboratories limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lamotrigine
Generic Name lamotrigine
Labeler dr.reddy's laboratories limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lamotrigine 25 mg/1

Manufacturer
Dr.Reddy's Laboratories Limited

Identifiers & Regulatory

Product NDC 55111-220
Product ID 55111-220_b59e510e-d6aa-6f6b-53ef-3152aeedced7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076708
Listing Expiration 2026-12-31
Marketing Start 2009-01-29

Pharmacologic Class

Established (EPC)
anti-epileptic agent [epc] mood stabilizer [epc]
Mechanism of Action
organic cation transporter 2 inhibitors [moa] dihydrofolate reductase inhibitors [moa]
Physiologic Effect
decreased central nervous system disorganized electrical activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55111220
Hyphenated Format 55111-220

Supplemental Identifiers

RxCUI
198427 198428 198429 282401
UPC
0355111222019 0355111223016 0355111221012
UNII
U3H27498KS
NUI
N0000175753 N0000008486 N0000175751 N0000187061 N0000000191

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 lamotrigine (source: ndc)
Generic Name lamotrigine (source: ndc)
Application Number ANDA076708 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (55111-220-01)
  • 500 TABLET in 1 BOTTLE (55111-220-05)
  • 30 TABLET in 1 BOTTLE (55111-220-30)
  • 60 TABLET in 1 BOTTLE (55111-220-60)
  • 10 BLISTER PACK in 1 CARTON (55111-220-78) / 10 TABLET in 1 BLISTER PACK (55111-220-79)
source: ndc

Packages (5)

55111-220-01 100 TABLET in 1 BOTTLE (55111-220-01) 55111-220-05 500 TABLET in 1 BOTTLE (55111-220-05) 55111-220-30 30 TABLET in 1 BOTTLE (55111-220-30) 55111-220-60 60 TABLET in 1 BOTTLE (55111-220-60) 55111-220-78 10 BLISTER PACK in 1 CARTON (55111-220-78) / 10 TABLET in 1 BLISTER PACK (55111-220-79)

Ingredients (1)

lamotrigine (25 mg/1)

Linked Drug Pages (1)

Lamotrigine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b59e510e-d6aa-6f6b-53ef-3152aeedced7", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "upc": ["0355111222019", "0355111223016", "0355111221012"], "unii": ["U3H27498KS"], "rxcui": ["198427", "198428", "198429", "282401"], "spl_set_id": ["44670496-41ea-36a1-c435-32e359766a74"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]", "Mood Stabilizer [EPC]"], "pharm_class_moa": ["Organic Cation Transporter 2 Inhibitors [MoA]", "Dihydrofolate Reductase Inhibitors [MoA]"], "manufacturer_name": ["Dr.Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (55111-220-01)", "package_ndc": "55111-220-01", "marketing_start_date": "20090129"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (55111-220-05)", "package_ndc": "55111-220-05", "marketing_start_date": "20090129"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (55111-220-30)", "package_ndc": "55111-220-30", "marketing_start_date": "20090129"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (55111-220-60)", "package_ndc": "55111-220-60", "marketing_start_date": "20090129"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (55111-220-78)  / 10 TABLET in 1 BLISTER PACK (55111-220-79)", "package_ndc": "55111-220-78", "marketing_start_date": "20090129"}], "brand_name": "Lamotrigine", "product_id": "55111-220_b59e510e-d6aa-6f6b-53ef-3152aeedced7", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Dihydrofolate Reductase Inhibitors [MoA]", "Mood Stabilizer [EPC]", "Organic Cation Transporter 2 Inhibitors [MoA]"], "product_ndc": "55111-220", "generic_name": "Lamotrigine", "labeler_name": "Dr.Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "25 mg/1"}], "application_number": "ANDA076708", "marketing_category": "ANDA", "marketing_start_date": "20090129", "listing_expiration_date": "20261231"}