American Pacific Corporation
NDC Database
American Pacific Corporation
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 32
- Latest Marketing Date 2025-05-05
- Data Source FDA
- First Marketing Date 1972-01-01
Company Overview
Social Profiles
Company Snapshot
American Pacific Corporation
3883 Howard Hughes Parkway Suite 700 Las Vegas, NV 89169 USA
U.S.A
www.apfc.com/ info@apfc.com View on MapNDC Records ( 32 records )
Nonproprietary Name
CARMUSTINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
CARMUSTINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1972-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
TEMOZOLOMIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
TEMOZOLOMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1999-08-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
TENOFOVIR DISOPROXIL FUMARATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
TENOFOVIR DISOPROXIL FUMARATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2001-10-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
LEVETIRACETAM
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
AMERICAN PACIFIC CORPORATION
Marketing Category
BULK INGREDIENT
Substance
LEVETIRACETAM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2001-03-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
RUXOLITINIB PHOSPHATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
RUXOLITINIB PHOSPHATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-08-16
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
THIOGUANINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
AMERICAN PACIFIC CORPORATION
Marketing Category
BULK INGREDIENT
Substance
THIOGUANINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-03-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
BUSULFAN
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
AMERICAN PACIFIC CORPORATION
Marketing Category
BULK INGREDIENT
Substance
BUSULFAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-10-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
CHLORAMBUCIL
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
AMERICAN PACIFIC CORPORATION
Marketing Category
BULK INGREDIENT
Substance
CHLORAMBUCIL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2001-05-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Melphalan
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
MELPHALAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2002-02-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sofosbuvir
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
SOFOSBUVIR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-05-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Brigatinib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
BRIGATINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-12-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
dex-Methylphenidate Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
DEXMETHYLPHENIDATE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2017-09-04
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
RUXOLITINIB PHOSPHATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
RUXOLITINIB PHOSPHATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2011-10-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Thiotepa
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
THIOTEPA
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-01-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Cyclophosphamide Monohydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
CYCLOPHOSPHAMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-05-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
TEMOZOLOMIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
TEMOZOLOMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1999-08-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Levorphanol Tartrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
LEVORPHANOL TARTRATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2019-12-06
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Melphalan, sieved
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
MELPHALAN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-03-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Crystalline RTA 408
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
OMAVELOXOLONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-02-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
APD334 L-Arginine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
ETRASIMOD ARGININE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-09-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Vibegron
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
VIBEGRON
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-10-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Finerenone
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
FINERENONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-04-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
LOXO-292
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
SELPERCATINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-11-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Remifentanil Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
REMIFENTANIL HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2020-10-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Oseltamivir Phosphate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
OSELTAMIVIR PHOSPHATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-04-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sotorasib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
SOTORASIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-11-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Labetalol Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
LABETALOL HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-04-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Molnupiravir
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
MOLNUPIRAVIR
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-11-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ruxolitinib phosphate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
RUXOLITINIB PHOSPHATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-11-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Acalabrutinib Maleate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
ACALABRUTINIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-08-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
LDF 3A
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
LISDEXAMFETAMINE DIMESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2025-05-05
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Etrasimod L-Arginine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
American Pacific Corporation
Marketing Category
BULK INGREDIENT
Substance
ETRASIMOD ARGININE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-09-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
32 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).
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NDC
50683-0017
Nonproprietary Name
CARMUSTINE
Labeler
American Pacific Corporation
Dosage Form
POWDER
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