pamidronate disodium

Generic: pamidronate disodium

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pamidronate disodium
Generic Name pamidronate disodium
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

pamidronate disodium 6 mg/mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 61703-325
Product ID 61703-325_0bc105d8-d6f2-4632-8b97-70fecc2783d1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075841
Listing Expiration 2026-12-31
Marketing Start 2003-07-28

Pharmacologic Class

Classes
bisphosphonate [epc] diphosphonates [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 61703325
Hyphenated Format 61703-325

Supplemental Identifiers

RxCUI
1737449 1737451 1737453
UNII
8742T8ZQZA

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 pamidronate disodium (source: ndc)
Generic Name pamidronate disodium (source: ndc)
Application Number ANDA075841 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 6 mg/mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (61703-325-18) / 10 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

Ingredients (1)

pamidronate disodium (6 mg/mL)

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 (61703-325-18)  / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "61703-325-18", "marketing_start_date": "20030728"}], "brand_name": "Pamidronate Disodium", "product_id": "61703-325_0bc105d8-d6f2-4632-8b97-70fecc2783d1", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "61703-325", "generic_name": "PAMIDRONATE DISODIUM", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pamidronate Disodium", "active_ingredients": [{"name": "PAMIDRONATE DISODIUM", "strength": "6 mg/mL"}], "application_number": "ANDA075841", "marketing_category": "ANDA", "marketing_start_date": "20030728", "listing_expiration_date": "20261231"}