Package 46708-096-30

Brand: lamotrigine

Generic: lamotrigine chewable dispersible
NDC Package

Package Facts

Identity

Package NDC 46708-096-30
Digits Only 4670809630
Product NDC 46708-096
Description

30 TABLET, FOR SUSPENSION in 1 BOTTLE (46708-096-30)

Marketing

Marketing Status
Marketed Since 2016-01-29
Brand lamotrigine
Generic lamotrigine chewable dispersible
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ea08829-6e98-4a5f-97d0-da2d1ac96dc1", "openfda": {"nui": ["N0000175753", "N0000008486", "N0000175751", "N0000187061", "N0000000191"], "upc": ["0346708096304", "0346708095307"], "unii": ["U3H27498KS"], "rxcui": ["311264", "311265"], "spl_set_id": ["ae6522d4-d824-44aa-afe0-70cdcbd845af"], "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": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FOR SUSPENSION in 1 BOTTLE (46708-096-30)", "package_ndc": "46708-096-30", "marketing_start_date": "20160129"}, {"sample": false, "description": "100 TABLET, FOR SUSPENSION in 1 BOTTLE (46708-096-31)", "package_ndc": "46708-096-31", "marketing_start_date": "20160129"}, {"sample": false, "description": "1000 TABLET, FOR SUSPENSION in 1 BOTTLE (46708-096-91)", "package_ndc": "46708-096-91", "marketing_start_date": "20160129"}], "brand_name": "lamotrigine", "product_id": "46708-096_4ea08829-6e98-4a5f-97d0-da2d1ac96dc1", "dosage_form": "TABLET, FOR SUSPENSION", "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": "46708-096", "generic_name": "lamotrigine chewable dispersible", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "lamotrigine", "active_ingredients": [{"name": "LAMOTRIGINE", "strength": "25 mg/1"}], "application_number": "ANDA201168", "marketing_category": "ANDA", "marketing_start_date": "20160129", "listing_expiration_date": "20261231"}