Package 63304-440-09
Brand: risedronate sodium
Generic: risedronate sodiumPackage Facts
Identity
Package NDC
63304-440-09
Digits Only
6330444009
Product NDC
63304-440
Description
1 DOSE PACK in 1 CARTON (63304-440-09) / 4 TABLET, DELAYED RELEASE in 1 DOSE PACK (63304-440-11)
Marketing
Marketing Status
Brand
risedronate sodium
Generic
risedronate sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d97c9e6a-01e9-46ae-9088-0ca86b4eb842", "openfda": {"unii": ["OFG5EXG60L"], "rxcui": ["1020064", "1020065"], "spl_set_id": ["1d9e520b-2fa6-4603-b397-f0fc24fae775"], "manufacturer_name": ["Sun Pharmaceutical Industires Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 DOSE PACK in 1 CARTON (63304-440-09) / 4 TABLET, DELAYED RELEASE in 1 DOSE PACK (63304-440-11)", "package_ndc": "63304-440-09", "marketing_start_date": "20190710"}], "brand_name": "RISEDRONATE SODIUM", "product_id": "63304-440_d97c9e6a-01e9-46ae-9088-0ca86b4eb842", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "63304-440", "generic_name": "RISEDRONATE SODIUM", "labeler_name": "Sun Pharmaceutical Industires Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RISEDRONATE SODIUM", "active_ingredients": [{"name": "RISEDRONATE SODIUM", "strength": "35 mg/1"}], "application_number": "ANDA203925", "marketing_category": "ANDA", "marketing_start_date": "20190710", "listing_expiration_date": "20261231"}