pamidronate disodium
Generic: pamidronate disodium
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
pamidronate disodium
Generic Name
pamidronate disodium
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
pamidronate disodium 3 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
61703-324
Product ID
61703-324_0bc105d8-d6f2-4632-8b97-70fecc2783d1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075841
Listing Expiration
2026-12-31
Marketing Start
2005-10-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
61703324
Hyphenated Format
61703-324
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
pamidronate disodium (source: ndc)
Generic Name
pamidronate disodium (source: ndc)
Application Number
ANDA075841 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3 mg/mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (61703-324-18) / 10 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0bc105d8-d6f2-4632-8b97-70fecc2783d1", "openfda": {"unii": ["8742T8ZQZA"], "rxcui": ["1737449", "1737451", "1737453"], "spl_set_id": ["9b6a9a3b-71c9-4dcb-b857-5d1de25c3a23"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (61703-324-18) / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "61703-324-18", "marketing_start_date": "20051001"}], "brand_name": "Pamidronate Disodium", "product_id": "61703-324_0bc105d8-d6f2-4632-8b97-70fecc2783d1", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "61703-324", "generic_name": "PAMIDRONATE DISODIUM", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pamidronate Disodium", "active_ingredients": [{"name": "PAMIDRONATE DISODIUM", "strength": "3 mg/mL"}], "application_number": "ANDA075841", "marketing_category": "ANDA", "marketing_start_date": "20051001", "listing_expiration_date": "20261231"}