ibandronate sodium

Generic: ibandronate sodium

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibandronate sodium
Generic Name ibandronate sodium
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ibandronate sodium 150 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7654
Product ID 50090-7654_1b55f284-94ab-46b3-bb1b-0ef5746bb901
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078997
Listing Expiration 2026-12-31
Marketing Start 2012-06-21

Pharmacologic Class

Classes
bisphosphonate [epc] diphosphonates [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907654
Hyphenated Format 50090-7654

Supplemental Identifiers

RxCUI
904932
UNII
J12U072QL0

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 ibandronate sodium (source: ndc)
Generic Name ibandronate sodium (source: ndc)
Application Number ANDA078997 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (50090-7654-0) / 3 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

50090-7654-0 1 BLISTER PACK in 1 CARTON (50090-7654-0) / 3 TABLET in 1 BLISTER PACK

Ingredients (1)

ibandronate sodium (150 mg/1)

Linked Drug Pages (1)

Ibandronate sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1b55f284-94ab-46b3-bb1b-0ef5746bb901", "openfda": {"unii": ["J12U072QL0"], "rxcui": ["904932"], "spl_set_id": ["e5b6c2a9-a55f-41f9-a592-e26ef03e2d73"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50090-7654-0)  / 3 TABLET in 1 BLISTER PACK", "package_ndc": "50090-7654-0", "marketing_start_date": "20250917"}], "brand_name": "Ibandronate sodium", "product_id": "50090-7654_1b55f284-94ab-46b3-bb1b-0ef5746bb901", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "50090-7654", "generic_name": "Ibandronate sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibandronate sodium", "active_ingredients": [{"name": "IBANDRONATE SODIUM", "strength": "150 mg/1"}], "application_number": "ANDA078997", "marketing_category": "ANDA", "marketing_start_date": "20120621", "listing_expiration_date": "20261231"}