POLYETHYLENE GLYCOL 2000
UNII HAF0412YIT

Substance Identification & Data

This profile provides standardized clinical and technical data for Polyethylene Glycol 2000, uniquely identified by the FDA Unique Ingredient Identifier (UNII) HAF0412YIT.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 25322-68-3 and the RxNorm Concept ID (RxCUI) 1364383. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
HAF0412YIT
CAS Registry Number
25322-68-3
RxNorm Concept ID
1364383

Detailed Substance Profile

Preferred Name
POLYETHYLENE GLYCOL 2000
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
HAF0412YIT
The specific atomic composition represented as a molecular structure string.
Substance Type
polymer
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Polyethylene Glycol 2000. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.

FDA Official Name

PEG-45

Common Names & Synonyms

MACROGOL 2000
PEG 2000
POLYETHYLENE GLYCOL (45)
POLYETHYLENE GLYCOL 2000

Brand / Trade Names

PEG-2000
POLYGLYKOL 2000

NDC Products Containing POLYETHYLENE GLYCOL 2000

This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory:

Manufacturer Quick Index

→ A-S Medication Solutions 8
→ ASTONEA LABS PRIVATE LIMITED 1
→ Acme United Corporation 2
→ Advanced Rx of Tennessee, LLC 1
→ Ajanta Pharma USA Inc. 3
→ Blenheim Pharmacal, Inc. 2
→ Bryant Ranch Prepack 10
→ Cambridge Therapeutics Technologies, LLC 1
→ Carlsbad Technology, Inc. 6
→ Cellinbio Co Ltd 1
→ Direct RX 2
→ DirectRx 1
→ Direct_Rx 2
→ Golden State Medical Supply, Inc. 5
→ Guangzhou Kadiya Biotechnology Co., Ltd. 1
→ HANCHOYEANBIOTEC Co.,Ltd. 1
→ Ingenus Pharmaceuticals, LLC 3
→ Northwind Health Company, LLC 2
→ NuCare Pharmaceuticals, Inc. 1
→ NuCare Pharmaceuticals,Inc. 3
→ PBM Pharmaceuticals, Inc 1
→ PHOENIX RX LLC 1
→ Preferred Pharmaceuticals Inc. 2
→ Proficient Rx LP 4
→ PureTek Corporation 1
→ Quantum, Inc. 1
→ REMEDYREPACK INC. 5
→ REPHARM LLC 2
→ RPK Pharmaceuticals, Inc. 2
→ Rebel Distributors Corp 1
→ RedPharm Drug, Inc. 3
→ Redpharm Drug 1
→ St. Mary's Medical Park Pharmacy 1
→ Sterling-Knight Pharmaceuticals, LLC 1
→ Supernus Pharmaceuticals, Inc. 3
→ THE KROGER CO 1
→ Umedica Laboratories USA Inc. 3
→ Unit Dose Services 2
→ Xiamen Olivee Daily Use Chemical Co., Ltd. 7
→ medsource pharmaceuticals 1

A-S Medication Solutions

NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 50090-0542

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 50090-0543

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 50090-0545

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 50090-7818

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 50090-7838

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 50090-7839

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 50090-7880

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 50090-7881

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

ASTONEA LABS PRIVATE LIMITED

NDC Product

Astonea Cold Therapy
NDC 77338-007

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH DRUG
Inactive / Discontinued

Acme United Corporation

NDC Product
Human Otc Drug

Physicianscare Allergy Antihistamine
NDC 0924-0056

Generic Name
Diphenhydramine Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Physicianscare Sinus Non-drowsy
NDC 0924-0133

Generic Name
Phenylephrine Hcl
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Advanced Rx of Tennessee, LLC

NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 80425-0569

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Ajanta Pharma USA Inc.

NDC Product

Oxcarbazepine
NDC 27241-304

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
NDA AUTHORIZED GENERIC
Inactive / Discontinued
NDC Product

Oxcarbazepine
NDC 27241-305

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
NDA AUTHORIZED GENERIC
Inactive / Discontinued
NDC Product

Oxcarbazepine
NDC 27241-306

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
NDA AUTHORIZED GENERIC
Inactive / Discontinued

Blenheim Pharmacal, Inc.

Bryant Ranch Prepack

NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 63629-2010

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 63629-2011

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 63629-2012

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 63629-2013

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 63629-2077

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 71335-0357

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 71335-0481

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 72162-1733

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 72162-1734

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Cambridge Therapeutics Technologies, LLC

Carlsbad Technology, Inc.

NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 61442-101

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 61442-102

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 61442-103

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 61442-226

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 61442-227

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Cellinbio Co Ltd

NDC Product

Suyan Jeongbaek
NDC 76173-1007

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH FINAL
Inactive / Discontinued

Direct RX

NDC Product

Diclofenac Sodium D/r
NDC 61919-074

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
ANDA
Active Listing
NDC Product

Diclofenac Sodium D/r
NDC 61919-075

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
ANDA
Active Listing

DirectRx

NDC Product
Human Prescription Drug

Diclofenac Sodium D/r
NDC 72189-675

Generic Name
Diclofenac Sodium D/r
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Direct_Rx

NDC Product

Diclofenac Sodium D/r
NDC 61919-075

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
ANDA
Inactive / Discontinued
NDC Product

Diclofenac Sodium D/r
NDC 61919-075

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
ANDA
Inactive / Discontinued

Golden State Medical Supply, Inc.

NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 51407-536

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 51407-537

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 51407-538

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 51407-967

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 51407-968

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Guangzhou Kadiya Biotechnology Co., Ltd.

HANCHOYEANBIOTEC Co.,Ltd.

Ingenus Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Oxcarbazepine
NDC 50742-611

Generic Name
Oxcarbazepine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxcarbazepine
NDC 50742-612

Generic Name
Oxcarbazepine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxcarbazepine
NDC 50742-613

Generic Name
Oxcarbazepine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Northwind Health Company, LLC

NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 51655-176

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 51655-280

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

NuCare Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 68071-3184

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

NuCare Pharmaceuticals,Inc.

NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 68071-4117

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 68071-4231

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 68071-4934

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

PBM Pharmaceuticals, Inc

NDC Product

Donnatal Extentabs
NDC 66213-421

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued

PHOENIX RX LLC

NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 85509-1103

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Preferred Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 68788-8952

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 68788-9806

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Proficient Rx LP

NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 63187-222

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 71205-494

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 71205-991

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 71205-995

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

PureTek Corporation

NDC Product
Human Prescription Drug

Inflammacin
NDC 59088-093

Generic Name
Diclofenac Sodium, Capsaicin
Dosage Form
Kit
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Quantum, Inc.

NDC Product
Human Otc Drug

Buzz Away Sting Soothe
NDC 70084-810

Generic Name
Menthol
Dosage Form
Liquid
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

REMEDYREPACK INC.

NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 70518-0627

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 70518-0756

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 70518-1104

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 70518-2707

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 70518-4602

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

REPHARM LLC

NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 61145-101

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 61145-102

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

RPK Pharmaceuticals, Inc.

Rebel Distributors Corp

RedPharm Drug, Inc.

NDC Product
Human Prescription Drug

Diclofenac Sodium
NDC 67296-1197

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Redpharm Drug

NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 67296-2215

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

St. Mary's Medical Park Pharmacy

Sterling-Knight Pharmaceuticals, LLC

NDC Product

Flexipak
NDC 69336-202

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
ANDA
Inactive / Discontinued

Supernus Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Oxtellar Xr
NDC 17772-121

Generic Name
Oxcarbazepine
Dosage Form
Tablet
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Oxtellar Xr
NDC 17772-122

Generic Name
Oxcarbazepine
Dosage Form
Tablet
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Oxtellar Xr
NDC 17772-123

Generic Name
Oxcarbazepine
Dosage Form
Tablet
Route
Oral
Marketing
NDA
Active Listing

THE KROGER CO

Umedica Laboratories USA Inc.

NDC Product
Human Prescription Drug

Diclofenac Sodium
NDC 60290-082

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium
NDC 60290-083

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium
NDC 60290-084

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Unit Dose Services

Xiamen Olivee Daily Use Chemical Co., Ltd.

NDC Product

Spatheraphy
NDC 56136-001

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Spatheraphy
NDC 56136-002

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Spatheraphy
NDC 56136-003

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Spatheraphy
NDC 56136-004

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Spatheraphy
NDC 56136-005

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Spatheraphy
NDC 56136-006

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Spatheraphy
NDC 56136-007

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued

medsource pharmaceuticals

External Clinical & Regulatory Resources

CAS
Common Chemistry
NCATS
Inxight Drugs
NLM
DailyMed Products
NCATS
GSRS Full Record