Purisys LLC
NDC Database

Purisys LLC

NDC Database

National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.

Bulk Ingredient
  • Total Records 9
  • Latest Marketing Date 2026-03-02
  • Data Source FDA
  • First Marketing Date 2020-03-11
Company Overview

Company

Purisys LLC

Country

U.S.A

Website

Visit Website

Email

aambrosi@Noramco.com

Social Profiles

LinkedIn
Company Snapshot

Purisys LLC

1550 Olympic Drive, Athens GA 30601

U.S.A

purisys.com/ aambrosi@Noramco.com View on Map
NDC Records ( 9 records )
2021
30 Jul
Bulk Ingredient NDC: 73548-0057

Nonproprietary Name

Hydromorphone Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Purisys LLC

Marketing Category

BULK INGREDIENT

73548-0057

Substance

HYDROMORPHONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2021-07-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2026
02 Mar
Bulk Ingredient NDC: 73548-1060

Nonproprietary Name

Naltrexone Base

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Purisys LLC

Marketing Category

BULK INGREDIENT

73548-1060

Substance

NALTREXONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-03-02

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2021
01 Mar
Bulk Ingredient NDC: 73548-2155

Nonproprietary Name

Cannabidiol

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Purisys LLC

Marketing Category

BULK INGREDIENT

73548-2155

Substance

CANNABIDIOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-03-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
11 Mar
Bulk Ingredient NDC: 73548-2162

Nonproprietary Name

Nabilone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Purisys LLC

Marketing Category

BULK INGREDIENT

73548-2162

Substance

NABILONE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2020-03-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
01 May
Bulk Ingredient NDC: 73548-2193

Nonproprietary Name

Dexmethylphenidate Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Purisys LLC

Marketing Category

BULK INGREDIENT

73548-2193

Substance

DEXMETHYLPHENIDATE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2025-05-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
15 Oct
Bulk Ingredient NDC: 73548-2200

Nonproprietary Name

Dronabinol in Sesame Oil

Dosage Form

OIL

Strength

0.2 kg/.2kg

Labeler

Purisys LLC

Marketing Category

BULK INGREDIENT

73548-2200

Substance

DRONABINOL

Product Type

BULK INGREDIENT

DEA Schedule

CI

Start Marketing Date

2021-10-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
08 Mar
Bulk Ingredient NDC: 73548-2358

Nonproprietary Name

Dronabinol

Dosage Form

OIL

Strength

1 kg/kg

Labeler

Purisys LLC

Marketing Category

BULK INGREDIENT

73548-2358

Substance

DRONABINOL

Product Type

BULK INGREDIENT

DEA Schedule

CI

Start Marketing Date

2021-03-08

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
02 Sep
Bulk Ingredient NDC: 73548-8019

Nonproprietary Name

Nalmefene Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Purisys LLC

Marketing Category

BULK INGREDIENT

73548-8019

Substance

NALMEFENE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-09-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
01 Dec
Bulk Ingredient NDC: 73548-8031

Nonproprietary Name

Powdered Opium

Dosage Form

POWDER

Strength

0.1 kg/.1kg

Labeler

Purisys LLC

Marketing Category

BULK INGREDIENT

73548-8031

Substance

MORPHINE

Product Type

BULK INGREDIENT

DEA Schedule

CII

Start Marketing Date

2023-12-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
9 total
  • Bulk Ingredient
Official Source

NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).

Visit FDA NDC Directory
NDC Record Details Preview

Explore important National Drug Code information available in the records above.

NDC

73548-0057

Nonproprietary Name

Hydromorphone Hydrochloride

Labeler

Purisys LLC

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized NDC records

NDC data is based on publicly available U.S. Food and Drug Administration (FDA) National Drug Code information.

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