Package 29300-139-01

Brand: divalproex sodium

Generic: divalproex sodium
NDC Package

Package Facts

Identity

Package NDC 29300-139-01
Digits Only 2930013901
Product NDC 29300-139
Description

100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-01)

Marketing

Marketing Status
Marketed Since 2011-10-01
Brand divalproex sodium
Generic divalproex sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "674e58bd-f580-4805-a7e2-febcaa37bca5", "openfda": {"upc": ["0329300140019"], "unii": ["644VL95AO6"], "rxcui": ["1099625", "1099678", "1099870"], "spl_set_id": ["1ec1a441-218a-4c80-a0cb-69bcc327f472"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-01)", "package_ndc": "29300-139-01", "marketing_start_date": "20111001"}, {"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-05)", "package_ndc": "29300-139-05", "marketing_start_date": "20111001"}, {"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-10)", "package_ndc": "29300-139-10", "marketing_start_date": "20111001"}], "brand_name": "Divalproex Sodium", "product_id": "29300-139_674e58bd-f580-4805-a7e2-febcaa37bca5", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "29300-139", "generic_name": "Divalproex Sodium", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA079163", "marketing_category": "ANDA", "marketing_start_date": "20111001", "listing_expiration_date": "20261231"}