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NUCLEAR DIAGNOSTIC PRODUCTS OF PHILADELPHIA, INC

UEI: QJKJD5FKTNP3CAGE: 6XCB6

NUCLEAR DIAGNOSTIC PRODUCTS OF PHILADELPHIA, INC is a federal contractor, registered under UEI QJKJD5FKTNP3 and CAGE code 6XCB6. It has been awarded $6,312,869 in federal contracts. Primary work spans Pharmaceutical Preparation Manufacturing. Top awarding agencies include Department Of Veterans Affairs.

Contact Information

Registration and classification details

Registration

UEI Code

QJKJD5FKTNP3

CAGE Code

6XCB6

Entity Structure

Corporate Entity (Not Tax Exempt)

Established

N/A

Business Classifications

For Profit Organization

NAICS Codes

325412Pharmaceutical Preparation Manufacturing(Primary)
424210Drugs and Druggists' Sundries Merchant Wholesalers
456110Pharmacies and Drug Retailers

Federal Contracting Overview

Award totals, agency breakdown, NAICS distribution, and geographic footprint.

AI Capability Profile

NUCLEAR DIAGNOSTIC PRODUCTS OF PHILADELPHIA, INC specializes in the manufacturing of radiopharmaceuticals for diagnostic imaging, with a focused expertise in the production of targeted radiolabeled compounds used in nuclear medicine. The company’s core capabilities center on GMP-compliant radiopharm...

NUCLEAR DIAGNOSTIC PRODUCTS OF PHILADELPHIA, INC specializes in the manufacturing of radiopharmaceuticals for diagnostic imaging, with a focused expertise in the production of targeted radiolabeled compounds used in nuclear medicine. The company’s core capabilities center on GMP-compliant radiopharmaceutical synthesis, isotopic labeling, and sterile formulation of agents such as ILLUCCIX and GA68, which are administered for positron emission tomography (PET) and other molecular imaging applications. Their technical proficiency includes radiolysis control, cold kit reconstitution, automated synthesis modules, and strict adherence to USP <825> standards for radiopharmaceutical handling. The firm demonstrates a specialized niche in producing short-lived, high-specific-activity agents requiring precise radiochemical purity and rapid distribution logistics, positioning them as a critical supplier in the diagnostic nuclear medicine supply chain. The company maintains a consistent and enduring relationship with the Department of Veterans Affairs, supplying FDA-approved radiopharmaceuticals to VA medical centers nationwide for oncology, cardiology, and neurology diagnostics. This recurring engagement reflects a trusted, mission-critical partnership built on reliable product delivery, regulatory compliance, and adherence to VA-specific procurement protocols for nuclear pharmacy services. Operating under NAICS 325412, the firm is deeply embedded in the pharmaceutical preparation manufacturing sector, with a vertical specialization in radiopharmaceuticals rather than traditional small-molecule or biologic drugs. This focus places them at the intersection of nuclear science, oncology diagnostics, and precision medicine, serving a high-regulation, low-volume, high-precision market segment. As a small business structured as a 2L entity based in Cherry Hill, New Jersey, the company operates without federal certifications such as 8(a), HUBZone, or SDVOSB. Its geographic footprint is centered in the Mid-Atlantic region, with a national supply footprint supporting federal healthcare delivery systems through specialized radiopharmaceutical manufacturing.

Key Performance Metrics

Awards Count

13

All time

Active

3

Currently performing

Completed

10

Past period of performance

Total Awards

All time

Contracts

Prime · all time

Subcontracts

Sub · all time

Grants

Prime · all time

Subgrants

Sub · all time

Award Analytics & Distribution

Awards by Agency
Awards by NAICS
Awards by Agency Over Time
Awards by Place of Performance

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NAICS: 325412
New
Federal
Atropine Auto-Injector
Solicitation # SPE2DP-27-R-ATRO
DLA Troop Support is conducting market research via a sources sought notice for the procurement of Atropine Auto-Injectors under solicitation SPE2DP-27-ATRO. The agency intends to award a firm-fixed price, indefinite delivery, indefinite quantity contract consisting of a one-year base term and four one-year option terms. The required devices must deliver 1.67 mg of atropine base (equivalent to 2 mg atropine sulfate) and be 99.5 percent reliable, with a dispensing time of 0.5 seconds and an activation force between 0.90 and 3.60 kg. All products must be FDA approved per NDA No. 212319, comply with USP sterility standards, and maintain a minimum shelf life of 24 months upon delivery to DLA Distribution Susquehanna in New Cumberland, Pennsylvania. Strict packaging and marking requirements are mandated, including individual sealed polyethylene bags, intermediate boxes of 40 units, and exterior containers of 480 units, all conforming to MIL-STD-2073-1 and ASTM D4169-16. Labels must include specific dosage, storage, and usage instructions for nerve agent and insecticide poisoning. Interested respondents must provide their CAGE code, business size under NAICS 325412, and certification of commerciality per FAR 2.101. Manufacturers must submit FDA registration, while authorized distributors must provide a letter of commitment from the manufacturer. Responses are due by December 1, 2026.
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