HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%)
UNII 8136Y38GY5

Substance Identification & Data

This profile provides standardized clinical and technical data for Hydroxyethyl Cellulose (140 Mpa.s At 5%), uniquely identified by the FDA Unique Ingredient Identifier (UNII) 8136Y38GY5.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9004-62-0 and the RxNorm Concept ID (RxCUI) 1305727. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
8136Y38GY5
CAS Registry Number
9004-62-0
RxNorm Concept ID
1305727

Detailed Substance Profile

Preferred Name
HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%)
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
8136Y38GY5
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
C83767
National Cancer Institute reference terminology for clinical and research data.
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 Hydroxyethyl Cellulose (140 Mpa.s At 5%). 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.

Common Names & Synonyms

HYDROXYETHYL CELLULOSE (140 CPS AT 5%)
HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%)
HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%) [II]
HYDROXYETHYL CELLULOSE (140 MPA.S FOR 5% AQUEOUS SOLUTION)
HYDROXYETHYL CELLULOSE 250L
HYDROXYPROPYL ETHYLCELLULOSE 250L
HYDROXYPROPYL ETHYLCELLULOSE 250L [II]

Brand / Trade Names

CELLOSIZE EP 09
CELLOSIZE HEC EP 09
CELLOSIZE HEC WP/QP 09H
CELLOSIZE HEC WP/QP 09L
CELLOSIZE WP/QP 09H
HEC DAICEL SP200
NATROSOL 250 L
NATROSOL 250 LR
NATROSOL 250LR
NATROSOL HEC L PHARM

NDC Products Containing HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%)

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

Manufacturer Quick Index

Note: Due to the high number of listings (250), only Active Listings are currently displayed.
→ A-S Medication Solutions 2
→ AAA Pharmaceutical, Inc. 2
→ AMERIFOODS TRADING COMPANY 1
→ AMERISOURCE BERGEN 2
→ ANI Pharmaceuticals, Inc. 1
→ ATLANTIC BIOLOGICALS CORP. 1
→ Allegiant Health 1
→ Amazon.com Services LLC 1
→ American Health Packaging 3
→ Amici Pharma Inc. 1
→ Aphena Pharma Solutions - Tennessee, LLC 3
→ Apotex Corp 3
→ Ascend Laboratories, LLC 2
→ Asclemed USA, Inc. 1
→ Atlantic Biologicals Corp 1
→ Aurohealth LLC 2
→ BETTER LIVING BRANDS, LLC 1
→ Better Living Brands, LLC 1
→ Bi-Mart 1
→ Bionpharma Inc. 1
→ Blaine Labs Inc. 2
→ BluePoint Laboratories 5
→ Boscia LLC 1
→ Bryant Ranch Prepack 14
→ CHAIN DRUG MARKETING ASSOCIATION, INC. 2
→ CVS Pharmacy, Inc. 2
→ Cardinal Health 107, LLC 1
→ Cypress Pharmaceutical, Inc. 1
→ DISCOUNT DRUG MART 1
→ DOLGENCORP, INC. 2
→ EPIC PHARMA, LLC 1
→ Extra Shade, LLC 1
→ FAMILY DOLLAR 1
→ FSA STORE INC. 2
→ GERI-CARE PHARMACEUTICAL CORP 1
→ Glenmark Pharmaceuticals Inc., USA 4
→ Golden State Medical Supply, Inc. 1
→ Granules India Limited 2
→ Granules Pharmaceuticals Inc. 1
→ Grocery Outlet, Inc. 1
→ HARRIS TEETER 1
→ HEB 1
→ HYVEE INC 2
→ Haleon US Holdings LLC 1
→ Henan Toudaorong Biotechnology Co., Ltd. 1
→ Hikma Pharmaceuticals USA Inc. 2
→ Ingenus Pharmaceuticals, LLC 3
→ KROGER COMPANY 3
→ Kenvue Brands LLC 2
→ Kesin Pharma 1
→ LEADER/ Cardinal Health 110, Inc 2
→ LEADER/ Cardinal Health 110, Inc. 2
→ Laclede, Inc. 2
→ Lupin Pharmaceuticals, Inc. 1
→ MARC GLASSMAN, INC. 1
→ MARKSANS PHARMA LIMITED 1
→ MEIJER DISTRIBUTION INC 1
→ MEIJER, INC. 1
→ Major Pharmaceuticals 4
→ NCS HealthCare of KY, LLC dba Vangard Labs 1
→ NeilMed Pharmaceuticals Inc. 1
→ Neilmed Pharmaceuticals Inc. 2
→ Nite Storm LLC 1
→ Nivagen Pharmaceuticals, Inc. 2
→ Northstar Rx LLC 3
→ Northwind Health Company, LLC 1
→ Oceanside Pharmaceuticals 3
→ PAI Holdings, LLC dba PAI Pharma 8
→ PD-Rx Pharmaceuticals, Inc. 1
→ Pfizer Laboratories Div Pfizer Inc 4
→ Preferred Pharmaceuticals Inc. 2
→ Preferred Pharmaceuticals, Inc. 1
→ Proficient Rx LP 1
→ REMEDYREPACK INC. 1
→ RITE AID 3
→ Redpharm Drug 1
→ Rhodes Pharmaceuticals LLC 8
→ SAM'S WEST INC 1
→ STRATEGIC SOURCING SERVICES LLC 1
→ Scope Health Inc 1
→ Sun Pharmaceutical Industries, Inc. 1
→ TARGET CORPORATION 2
→ TIME CAP LABORATORIES, INC. 1
→ TOPCO ASSOCIATES LLC 1
→ U.S. Pharmaceuticals 3
→ United Natural Foods, Inc. dba UNFI 1
→ WAL-MART STORES INC 1
→ WALGREEN CO. 1
→ WALMART INC. 1
→ WINCO FOODS, LLC 1
→ Walgreens 1
→ Westminster Pharmaceuticals, LLC 1
→ Zydus Lifesciences Limited 3
→ Zydus Pharmaceuticals (USA) Inc. 3

A-S Medication Solutions

NDC Product
Human Prescription Drug

Prednisolone Sodium Phosphate
NDC 50090-1582

Generic Name
Prednisolone Sodium Phosphate
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nifedipine
NDC 50090-5284

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

AAA Pharmaceutical, Inc.

NDC Product
Human Otc Drug

Arthritis Pain
NDC 57344-200

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

8hr Muscle Aches And Pain
NDC 57344-201

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

AMERIFOODS TRADING COMPANY

NDC Product
Human Otc Drug

Arthritis Pain
NDC 61504-200

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

AMERISOURCE BERGEN

NDC Product
Human Otc Drug

8 Hour Arthritis Pain
NDC 46122-629

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

8 Hour Pain Relief
NDC 46122-630

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

ANI Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Naproxen Oral Suspension
NDC 70954-151

Generic Name
Naproxen Oral
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

ATLANTIC BIOLOGICALS CORP.

NDC Product
Human Prescription Drug

Prednisolone Sodium Phosphate
NDC 17856-0815

Generic Name
Prednisolone Sodium Phosphate
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

Allegiant Health

NDC Product
Human Otc Drug

Pain Relief
NDC 69168-461

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

Amazon.com Services LLC

NDC Product
Human Otc Drug

Amazon Basic Care Acetaminophen
NDC 72288-698

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

American Health Packaging

NDC Product
Human Otc Drug

Acetaminophen
NDC 60687-924

Generic Name
Acetaminophen
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate Extended Release
NDC 68084-157

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate Extended Release
NDC 68084-158

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Amici Pharma Inc.

NDC Product
Human Prescription Drug

Diclofenac Potassium
NDC 69292-550

Generic Name
Diclofenac Potassium
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Aphena Pharma Solutions - Tennessee, LLC

NDC Product
Human Prescription Drug

Nifedipine
NDC 71610-012

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

Nifedipine
NDC 71610-055

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

Nifedipine
NDC 71610-144

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

Apotex Corp

NDC Product
Human Prescription Drug

Fluvoxamine Maleate
NDC 60505-0164

Generic Name
Fluvoxamine Maleate
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fluvoxamine Maleate
NDC 60505-0165

Generic Name
Fluvoxamine Maleate
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fluvoxamine Maleate
NDC 60505-0166

Generic Name
Fluvoxamine Maleate
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Ascend Laboratories, LLC

NDC Product
Human Prescription Drug

Oxcarbazepine
NDC 67877-532

Generic Name
Oxcarbazepine
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rufinamide
NDC 67877-673

Generic Name
Rufinamide
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

Asclemed USA, Inc.

NDC Product
Human Otc Drug

Acetaminophen
NDC 76420-914

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

Atlantic Biologicals Corp

NDC Product
Human Prescription Drug

Prednisolone Sodium Phosphate
NDC 17856-8815

Generic Name
Prednisolone Sodium Phosphate
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

Aurohealth LLC

NDC Product
Human Otc Drug

Acetaminophen
NDC 58602-730

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

Acetaminophen
NDC 58602-873

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

BETTER LIVING BRANDS, LLC

NDC Product
Human Otc Drug

Arthritis Pain
NDC 21130-097

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

Better Living Brands, LLC

NDC Product
Human Otc Drug

Acetaminophen
NDC 21130-108

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

Bi-Mart

NDC Product
Human Otc Drug

Acetaminophen
NDC 37835-512

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

Bionpharma Inc.

NDC Product
Human Prescription Drug

Rufinamide
NDC 69452-223

Generic Name
Rufinamide
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

Blaine Labs Inc.

NDC Product
Human Otc Drug

Terpenicol Antifungal
NDC 63347-600

Generic Name
Undecylenic Acid
Dosage Form
Liquid
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Terpenicol
NDC 63347-601

Generic Name
Undecylenic Acid
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

BluePoint Laboratories

NDC Product
Human Otc Drug

Acetaminophen
NDC 68001-495

Generic Name
Acetaminophen
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Aprepitant
NDC 68001-666

Generic Name
Aprepitant
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Aprepitant
NDC 68001-667

Generic Name
Aprepitant
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Aprepitant
NDC 68001-668

Generic Name
Aprepitant
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Aprepitant
NDC 68001-669

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

Boscia LLC

NDC Product
Human Otc Drug

Oil-free Daily Hydration Spf 15
NDC 76151-105

Generic Name
Octinoxate, Avobenzone
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Bryant Ranch Prepack

NDC Product
Human Prescription Drug

Morphine Sulfate Er
NDC 63629-4483

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate
NDC 63629-4484

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate Extended Release
NDC 63629-8505

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nifedipine
NDC 63629-9109

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

Acetaminophen
NDC 71335-1340

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

Fluvoxamine Maleate
NDC 71335-1974

Generic Name
Fluvoxamine Maleate
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fluvoxamine Maleate
NDC 71335-2008

Generic Name
Fluvoxamine Maleate
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Acetaminophen
NDC 71335-9746

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

Morphine Sulfate Extended Release
NDC 72162-1352

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nifedipine
NDC 72162-1887

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

Ipratropium Bromide
NDC 72162-2143

Generic Name
Ipratropium Bromide
Dosage Form
Spray
Route
Nasal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Ipratropium Bromide
NDC 72162-2144

Generic Name
Ipratropium Bromide
Dosage Form
Spray
Route
Nasal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nifedipine
NDC 72162-2260

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

Nifedipine
NDC 72162-2261

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

CHAIN DRUG MARKETING ASSOCIATION, INC.

NDC Product
Human Otc Drug

8 Hour Pain Relief
NDC 83324-082

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

8 Hour Arthritis Pain
NDC 83324-083

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

CVS Pharmacy, Inc.

NDC Product
Human Otc Drug

Acetaminophen
NDC 69842-037

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

Acetaminophen
NDC 69842-635

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

Cardinal Health 107, LLC

NDC Product
Human Otc Drug

Guaifenesin
NDC 55154-5780

Generic Name
Guaifenesin
Dosage Form
Solution
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Cypress Pharmaceutical, Inc.

NDC Product
Human Prescription Drug

Sf
NDC 60258-151

Generic Name
1.1% Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing

DISCOUNT DRUG MART

NDC Product
Human Otc Drug

Arthritis Pain
NDC 53943-200

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

DOLGENCORP, INC.

NDC Product
Human Otc Drug

8 Hr Arthritis Pain Relief
NDC 55910-892

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

8 Hr Pain Relief
NDC 55910-895

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

EPIC PHARMA, LLC

NDC Product
Human Prescription Drug

Oxcarbazepine
NDC 42806-600

Generic Name
Oxcarbazepine
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

Extra Shade, LLC

FAMILY DOLLAR

NDC Product
Human Otc Drug

Acetaminophen
NDC 55319-185

Generic Name
Acetaminophen
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

FSA STORE INC.

NDC Product
Human Otc Drug

8hr Arthritis Pain
NDC 81522-200

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

8hr Muscle Aches And Pain
NDC 81522-201

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

GERI-CARE PHARMACEUTICAL CORP

NDC Product
Human Otc Drug

Acetaminophen
NDC 57896-268

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

Glenmark Pharmaceuticals Inc., USA

NDC Product
Human Prescription Drug

Aprepitant
NDC 68462-112

Generic Name
Aprepitant
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Aprepitant
NDC 68462-583

Generic Name
Aprepitant
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Aprepitant
NDC 68462-584

Generic Name
Aprepitant
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Aprepitant
NDC 68462-585

Generic Name
Aprepitant
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

Golden State Medical Supply, Inc.

NDC Product
Human Prescription Drug

Diclofenac Potassium
NDC 51407-443

Generic Name
Diclofenac Potassium
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Granules India Limited

NDC Product
Human Otc Drug

Acetaminophen
NDC 62207-183

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

Acetaminophen
NDC 62207-188

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

Granules Pharmaceuticals Inc.

NDC Product
Human Otc Drug

Acetaminophen
NDC 70010-160

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

Grocery Outlet, Inc.

NDC Product
Human Otc Drug

Arthritis Pain
NDC 85828-200

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

HARRIS TEETER

NDC Product
Human Otc Drug

8hr Arthritis Pain
NDC 72036-200

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

HEB

NDC Product
Human Otc Drug

Heb
NDC 37808-120

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

HYVEE INC

NDC Product
Human Otc Drug

Arthritis Pain
NDC 42507-205

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

Pain Relief
NDC 42507-303

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

Haleon US Holdings LLC

NDC Product
Human Otc Drug

Biotene
NDC 0135-0577

Generic Name
Sodium Monofluorophosphate
Dosage Form
Paste
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Henan Toudaorong Biotechnology Co., Ltd.

Hikma Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Ipratropium Bromide
NDC 0054-0045

Generic Name
Ipratropium Bromide
Dosage Form
Spray
Route
Nasal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Ipratropium Bromide
NDC 0054-0046

Generic Name
Ipratropium Bromide
Dosage Form
Spray
Route
Nasal
Marketing
ANDA
Active Listing

Ingenus Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Carbamazepine
NDC 50742-257

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

Carbamazepine
NDC 50742-258

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

Carbamazepine
NDC 50742-259

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

KROGER COMPANY

NDC Product
Human Otc Drug

Acetaminophen
NDC 30142-157

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

Arthritis Pain Relief
NDC 41226-699

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

8 Hour Pain Relief
NDC 41226-704

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

Kenvue Brands LLC

NDC Product
Human Otc Drug

Tylenol 8hr
NDC 50580-309

Generic Name
Acetaminophen
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

Tylenol 8 Hr Arthritis Pain
NDC 50580-783

Generic Name
Acetaminophen
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
NDA
Active Listing

Kesin Pharma

NDC Product
Human Prescription Drug

Prednisolone Sodium Phosphate
NDC 81033-021

Generic Name
Prednisolone Sodium Phosphate
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

LEADER/ Cardinal Health 110, Inc

NDC Product
Human Otc Drug

Acetaminophen
NDC 70000-0626

Generic Name
Acetaminophen
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Acetaminophen
NDC 70000-0627

Generic Name
Acetaminophen
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

LEADER/ Cardinal Health 110, Inc.

NDC Product
Human Otc Drug

8hr Arthritis Pain Relief
NDC 70000-0733

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

8hr Muscle Aches And Pain Relief
NDC 70000-0734

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

Laclede, Inc.

NDC Product
Human Otc Drug

Salivea
NDC 54897-701

Generic Name
Fluoride Toothpaste
Dosage Form
Paste, Dentifrice
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Salivea
NDC 54897-701

Generic Name
Fluoride Toothpaste
Dosage Form
Paste, Dentifrice
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing

Lupin Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Rufinamide
NDC 68180-797

Generic Name
Rufinamide
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

MARC GLASSMAN, INC.

NDC Product
Human Otc Drug

8 Hour Arthritis Pain
NDC 68998-401

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

MARKSANS PHARMA LIMITED

MEIJER DISTRIBUTION INC

NDC Product
Human Otc Drug

Acetaminophen
NDC 79481-0183

Generic Name
Acetaminophen
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

MEIJER, INC.

NDC Product
Human Otc Drug

Acetaminophen
NDC 79481-0184

Generic Name
Acetaminophen
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Major Pharmaceuticals

NDC Product
Human Prescription Drug

Morphine Sulfate Extended Release
NDC 0904-6557

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate Extended Release
NDC 0904-6558

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate Extended Release
NDC 0904-6559

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate Extended Release
NDC 0904-6560

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

NCS HealthCare of KY, LLC dba Vangard Labs

NDC Product
Human Otc Drug

Acetaminophen
NDC 0615-8624

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

NeilMed Pharmaceuticals Inc.

NDC Product
Human Otc Drug

Cooling Gel
NDC 13709-354

Generic Name
Pain Relief Cooling Gel
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Neilmed Pharmaceuticals Inc.

NDC Product
Human Otc Drug

Cooling Gel
NDC 13709-346

Generic Name
Pain Relief Cooling Gel
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Itch Relief
NDC 13709-351

Generic Name
Itch Relief Gel
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Nite Storm LLC

NDC Product
Human Otc Drug

Nite
NDC 85094-708

Generic Name
Personal Lubricant Lotion
Dosage Form
Oil
Route
Rectal; Vaginal
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Nivagen Pharmaceuticals, Inc.

Northstar Rx LLC

NDC Product
Human Prescription Drug

Carbamazepine
NDC 16714-063

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

Carbamazepine
NDC 16714-064

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

Carbamazepine
NDC 16714-065

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

Northwind Health Company, LLC

NDC Product
Human Prescription Drug

Nifedipine
NDC 51655-798

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

Oceanside Pharmaceuticals

NDC Product
Human Prescription Drug

Nifedipine
NDC 68682-105

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

Nifedipine
NDC 68682-106

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

Nifedipine
NDC 68682-107

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

PAI Holdings, LLC dba PAI Pharma

NDC Product
Human Otc Drug

Guaifenesin
NDC 0121-0744

Generic Name
Guaifenesin
Dosage Form
Solution
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription Drug

Prednisolone Sodium Phosphate
NDC 0121-0759

Generic Name
Prednisolone Sodium Phosphate
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Prednisolone Sodium Phosphate
NDC 0121-0773

Generic Name
Prednisolone Sodium Phosphate
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Prednisolone Sodium Phosphate
NDC 0121-0777

Generic Name
Prednisolone Sodium Phosphate
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Ondansetron
NDC 0121-0882

Generic Name
Ondansetron
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Guaifenesin
NDC 0121-1488

Generic Name
Guaifenesin
Dosage Form
Solution
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Guaifenesin
NDC 0121-1744

Generic Name
Guaifenesin
Dosage Form
Solution
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Guaifenesin
NDC 0121-2232

Generic Name
Guaifenesin
Dosage Form
Solution
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

PD-Rx Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Fluvoxamine Maleate
NDC 72789-221

Generic Name
Fluvoxamine Maleate
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Pfizer Laboratories Div Pfizer Inc

NDC Product
Human Prescription Drug

Xeljanz Xr
NDC 0069-0501

Generic Name
Tofacitinib
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Xeljanz Xr
NDC 0069-0502

Generic Name
Tofacitinib
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Xeljanz
NDC 0069-1002

Generic Name
Tofacitinib
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Xeljanz
NDC 0069-1029

Generic Name
Tofacitinib
Dosage Form
Solution
Route
Oral
Marketing
NDA
Active Listing

Preferred Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Prednisolone Sodium Phosphate
NDC 68788-4046

Generic Name
Prednisolone Sodium Phosphate
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fluvoxamine Maleate
NDC 68788-8175

Generic Name
Fluvoxamine Maleate
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Preferred Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Prednisolone Sodium Phosphate
NDC 68788-7708

Generic Name
Prednisolone Sodium Phosphate
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

Proficient Rx LP

NDC Product
Human Prescription Drug

Prednisolone Sodium Phosphate
NDC 63187-215

Generic Name
Prednisolone Sodium Phosphate
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

REMEDYREPACK INC.

NDC Product
Human Prescription Drug

Prednisolone Sodium Phosphate
NDC 70518-4524

Generic Name
Prednisolone Sodium Phosphate
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

RITE AID

NDC Product
Human Otc Drug

Acetaminophen
NDC 11822-5019

Generic Name
Acetaminophen
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Acetaminophen
NDC 11822-5019

Generic Name
Acetaminophen
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Acetaminophen
NDC 11822-5091

Generic Name
Acetaminophen
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Redpharm Drug

NDC Product
Human Prescription Drug

Prednisolone Sodium Phosphate
NDC 67296-2134

Generic Name
Prednisolone Sodium Phosphate
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

Rhodes Pharmaceuticals LLC

NDC Product
Human Prescription Drug

Ms Contin
NDC 42858-515

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

Ms Contin
NDC 42858-631

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

Ms Contin
NDC 42858-760

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

Morphine Sulfate Extended Release
NDC 42858-801

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate Extended Release
NDC 42858-802

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate Extended Release
NDC 42858-803

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate Extended Release
NDC 42858-804

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate Extended Release
NDC 42858-805

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

SAM'S WEST INC

NDC Product
Human Otc Drug

Acetaminophen
NDC 68196-935

Generic Name
Acetaminophen
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

STRATEGIC SOURCING SERVICES LLC

NDC Product
Human Otc Drug

8 Hour Pain Relief
NDC 70677-1123

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

Scope Health Inc

NDC Product
Human Otc Drug

Optase Allegro
NDC 72972-006

Generic Name
Hydroxyethyl Cellulose
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
OTC MONOGRAPH DRUG
Active Listing

Sun Pharmaceutical Industries, Inc.

NDC Product
Human Prescription Drug

Oxcarbazepine
NDC 51672-1393

Generic Name
Oxcarbazepine
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

TARGET CORPORATION

NDC Product
Human Otc Drug

Arthritis Pain Acetaminophen
NDC 11673-673

Generic Name
Acetaminophen
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

8hr Pain Relief
NDC 11673-928

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

TIME CAP LABORATORIES, INC.

NDC Product
Human Otc Drug

Acetaminophen
NDC 49483-699

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

TOPCO ASSOCIATES LLC

NDC Product
Human Otc Drug

Arthritis Pain Relief
NDC 36800-632

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

U.S. Pharmaceuticals

NDC Product
Human Prescription Drug

Xeljanz
NDC 63539-016

Generic Name
Tofacitinib
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Xeljanz Xr
NDC 63539-501

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

Xeljanz Xr
NDC 63539-502

Generic Name
Tofacitinib
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
NDA
Active Listing

United Natural Foods, Inc. dba UNFI

NDC Product
Human Otc Drug

Eight Hour Pain Relief
NDC 41163-203

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

WAL-MART STORES INC

NDC Product
Human Otc Drug

Acetaminophen
NDC 49035-181

Generic Name
Acetaminophen
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

WALGREEN CO.

NDC Product
Human Otc Drug

Acetaminophen
NDC 0363-9604

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

WALMART INC.

NDC Product
Human Otc Drug

Acetaminophen
NDC 79903-132

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

WINCO FOODS, LLC

NDC Product
Human Otc Drug

Arthritis Pain Relief
NDC 67091-401

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

Walgreens

NDC Product
Human Otc Drug

Acetaminophen
NDC 0363-0892

Generic Name
Acetaminophen
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Westminster Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Sodium Fluoride 1.1% Gel
NDC 69367-310

Generic Name
Sodium Fluoride
Dosage Form
Gel
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Zydus Lifesciences Limited

NDC Product
Human Prescription Drug

Carbamazepine
NDC 70771-1468

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

Carbamazepine
NDC 70771-1469

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

Carbamazepine
NDC 70771-1470

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

Zydus Pharmaceuticals (USA) Inc.

NDC Product
Human Prescription Drug

Carbamazepine
NDC 68382-555

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

Carbamazepine
NDC 68382-556

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

Carbamazepine
NDC 68382-557

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

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