risedronate sodium

Generic: risedronate sodium

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name risedronate sodium
Generic Name risedronate sodium
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

risedronate sodium monohydrate 5 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-3099
Product ID 0093-3099_5495c43b-77b2-4ac7-b138-7cac84cca3ba
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077132
Listing Expiration 2026-12-31
Marketing Start 2015-06-01

Pharmacologic Class

Classes
bisphosphonate [epc] diphosphonates [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00933099
Hyphenated Format 0093-3099

Supplemental Identifiers

RxCUI
905024 905032 905041 905092 905100
UNII
F67L43UT5C

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 risedronate sodium (source: ndc)
Generic Name risedronate sodium (source: ndc)
Application Number ANDA077132 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (0093-3099-56)
source: ndc

Packages (1)

Ingredients (1)

risedronate sodium monohydrate (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5495c43b-77b2-4ac7-b138-7cac84cca3ba", "openfda": {"unii": ["F67L43UT5C"], "rxcui": ["905024", "905032", "905041", "905092", "905100"], "spl_set_id": ["dddcd321-4d2e-4643-bf3c-7b752b33ba39"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0093-3099-56)", "package_ndc": "0093-3099-56", "marketing_start_date": "20150601"}], "brand_name": "Risedronate Sodium", "product_id": "0093-3099_5495c43b-77b2-4ac7-b138-7cac84cca3ba", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "0093-3099", "generic_name": "Risedronate Sodium", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Risedronate Sodium", "active_ingredients": [{"name": "RISEDRONATE SODIUM MONOHYDRATE", "strength": "5 mg/1"}], "application_number": "ANDA077132", "marketing_category": "ANDA", "marketing_start_date": "20150601", "listing_expiration_date": "20261231"}