SODIUM PHOSPHATE, DIBASIC, ANHYDROUS
UNII 22ADO53M6F

Substance Identification & Data

This profile provides standardized clinical and technical data for Sodium Phosphate, Dibasic, Anhydrous, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 22ADO53M6F.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 7558-79-4 and the RxNorm Concept ID (RxCUI) 314838. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
22ADO53M6F
CAS Registry Number
7558-79-4
RxNorm Concept ID
314838

Detailed Substance Profile

Preferred Name
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
22ADO53M6F
The specific atomic composition represented as a molecular structure string.
InChIKey
2Na.HO4P
International Chemical Identifier digital signature for unique molecular identification.
SMILES String
BNIILDVGGAEEIG-UHFFFAOYSA-L
Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
C66546
National Cancer Institute reference terminology for clinical and research data.
PubChem CID
24203
Unique identification number in the NCBI database of chemical substances.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
[O-]P(O)([O-])=O.[Na+].[Na+]

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Sodium Phosphate, Dibasic, Anhydrous. 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

DISODIUM PHOSPHATE

Common Names & Synonyms

ACETEST
DIBASIC SODIUM PHOSPHATE ANHYDROUS
DIBASIC SODIUM PHOSPHATE, ANHYDROUS
DISODIUM ACID PHOSPHATE
DISODIUM HYDROGEN PHOSPHATE ANHYDROUS
DISODIUM HYDROGEN PHOSPHATE, ANHYDROUS
DISODIUM PHOSPHATE [EP MONOGRAPH]
DISODIUM PHOSPHATE [HSDB]
DISODIUM PHOSPHATE, ANHYDROUS
EXSICCATED SODIUM PHOSPHATE
OSMOPREP COMPONENT SODIUM PHOSPHATE, DIBASIC ANHYDROUS
PHOSPHORIC ACID, DISODIUM SALT, ANHYDROUS
PHOSPHORIC ACID, SODIUM SALT (1:2)
SECONDARY SODIUM PHOSPHATE
SODIUM MONOHYDROGEN PHOSPHATE
SODIUM PHOSPHATE [FHFI]
SODIUM PHOSPHATE DIBASIC
SODIUM PHOSPHATE DIBASIC [WHO-DD]
SODIUM PHOSPHATE DIBASIC ANHYDROUS
SODIUM PHOSPHATE, DIBASIC [MI]
SODIUM PHOSPHATE, DIBASIC ANHYDROUS
SODIUM PHOSPHATE, DIBASIC ANHYDROUS [ORANGE BOOK]
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS [II]
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS [ORANGE BOOK]
SODIUM PHOSPHATE,DIBASIC,ANHYDROUS [VANDF]
VISICOL COMPONENT SODIUM PHOSPHATE, DIBASIC ANHYDROUS

Systematic Nomenclature

DISODIUM HYDROGEN MONOPHOSPHATE
DISODIUM HYDROGEN PHOSPHATE

Technical Codes

E-339(II)
FEMA NO. 2398
INS NO.339(II)
INS-339(II)

NDC Products Containing SODIUM PHOSPHATE, DIBASIC, ANHYDROUS

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 (500), only Active Listings are currently displayed. Display is limited to the first 200 products.
→ A-S Medication Solutions 5
→ ALK-ABELLO, INC. 1
→ ATLANTIC BIOLOGICALS CORP. 1
→ Acme United Corporation 1
→ Albertsons Companies 1
→ Alcon Laboratories, Inc. 2
→ Almay, Inc. 2
→ American Regent, Inc. 6
→ Amerisource Bergen 1
→ AmerisourceBergen Drug Corp 2
→ Aquestive Therapeutics 3
→ AstraZeneca Pharmaceuticals LP 1
→ Bausch & Lomb Incorporated 2
→ Baxter Healthcare Corporation 5
→ Beach Products, Inc. 1
→ Better Living Brands, LLC 1
→ Bioelements, Inc. 1
→ CLINIQUE LABORATORIES LLC 2
→ Camber Pharmaceuticals, Inc. 6
→ Chattem, Inc. 10
→ Church & Dwight Co., Inc. 6
→ Colgate-Palmolive - do not use 1
→ Colgate-Palmolive Company 1
→ Cosette Pharmaceuticals, Inc. 2
→ Dr. Reddy's Laboratories Inc 4
→ Dr. Reddy's Laboratories Inc. 3
→ Dr.Reddys Laboratories Inc 4
→ E.R. Squibb & Sons, L.L.C. 3
→ EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC) 1
→ Genentech, Inc. 2
→ Genomma Lab USA 1
→ H E B 9
→ HART Health 1
→ Haleon US Holdings LLC 4
→ Henry Schein, Inc. 1
→ Hikma Pharmaceuticals USA Inc. 3
→ Honeywell Safety Products, Inc. 1
→ Hospira, Inc. 2
→ Janssen Pharmaceuticals, Inc. 4
→ KROGER COMPANY 1
→ L'Oreal USA Products Inc 7
→ Lannett Company, Inc. 2
→ Lupin Pharmaceuticals,Inc. 1
→ L�Oreal USA Products Inc 1
→ Major Pharmaceuticals 1
→ Meijer Distribution, Inc. 2
→ Meijer, Inc. 7
→ Micro Labs Limited 1
→ NCS HealthCare of KY, LLC dba Vangard Labs 1
→ Nice-Pak Products, LLC 1
→ NorthStar RxLLC 1
→ Novartis Pharmaceuticals Corporation 3
→ PAI Holdings, LLC dba PAI Pharma 1
→ Padagis Israel Pharmaceuticals Ltd 1
→ Patrin Pharma, Inc. 1
→ Pfizer Laboratories Div Pfizer Inc 7
→ Pharmacia & Upjohn Company LLC 6
→ Rising Pharma Holdings, Inc. 2
→ Rite Aid Corporation 4
→ Rugby Laboratories 1
→ Sagent Pharmaceuticals 3
→ Sandoz Inc. 1
→ Sheffield Pharmaceuticals LLC 1
→ Sun Pharmaceutical Industries, Inc. 4
→ Target Corporation 5
→ The Kroger Co. 4
→ The Procter & Gamble Manufacturing Company 4
→ Topco Associates LLC 4
→ United Natural Foods, Inc. dba UNFI 3
→ Upsher-Smith Laboratories, LLC 1
→ WALGREEN COMPANY 1
→ WALGREENS CO. 1
→ Wal-Mart Stores,Inc., 1
→ Walgreen Co. 2
→ Walgreen Company 1
→ Walgreens Company 1
→ Walmart Inc. 4

A-S Medication Solutions

NDC Product
Human Prescription Drug

Latanoprost
NDC 50090-1920

Generic Name
Latanoprost
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Omeprazole
NDC 50090-5901

Generic Name
Omeprazole
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Omeprazole
NDC 50090-5902

Generic Name
Omeprazole
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Latanoprost
NDC 50090-7062

Generic Name
Latanoprost
Dosage Form
Solution
Route
Ophthalmic
Marketing
ANDA
Active Listing
NDC Product
Vaccine

Shingrix
NDC 50090-7919

Generic Name
Zoster Vaccine Recombinant, Adjuvanted
Dosage Form
Injection, Solution
Route
Intramuscular
Marketing
BLA
Active Listing

ALK-ABELLO, INC.

NDC Product
Human Prescription Drug

Pre-pen
NDC 49471-001

Generic Name
Benzylpenicilloyl Polylysine
Dosage Form
Injection
Route
Intradermal; Subcutaneous
Marketing
BLA
Active Listing

ATLANTIC BIOLOGICALS CORP.

NDC Product
Human Prescription Drug

Nystatin
NDC 17856-0508

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

Acme United Corporation

NDC Product
Human Otc Drug

Povidone-iodine
NDC 0924-5408

Generic Name
Povidone-iodine
Dosage Form
Solution
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Albertsons Companies

Alcon Laboratories, Inc.

NDC Product
Human Prescription Drug

Phenylephrine Hydrochloride
NDC 0065-0343

Generic Name
Phenylephrine Hydrochloride
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Phenylephrine Hydrochloride
NDC 0065-0349

Generic Name
Phenylephrine Hydrochloride
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
NDA
Active Listing

Almay, Inc.

American Regent, Inc.

NDC Product
Human Prescription Drug

Betamethasone Sodium Phosphate And Betamethasone Acetate
NDC 0517-0720

Generic Name
Betamethasone Sodium Phosphate And Betamethasone Acetate
Dosage Form
Injection, Suspension
Route
Intra-articular; Intralesional; Intramuscular
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Betamethasone Sodium Phosphate And Betamethasone Acetate
NDC 0517-0791

Generic Name
Betamethasone Sodium Phosphate And Betamethasone Acetate
Dosage Form
Injection, Suspension
Route
Intra-articular; Intralesional; Intramuscular
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Betamethasone Sodium Phosphate And Betamethasone Acetate
NDC 0517-0799

Generic Name
Betamethasone Sodium Phosphate And Betamethasone Acetate
Dosage Form
Injection, Suspension
Route
Intra-articular; Intralesional; Intramuscular
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Sodium Phosphates
NDC 0517-7305

Generic Name
Sodium Phosphate, Monobasic, Monohydrate And Sodium Phosphat...
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Sodium Phosphates
NDC 0517-7315

Generic Name
Sodium Phosphate, Monobasic, Monohydrate And Sodium Phosphat...
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Sodium Phosphates
NDC 0517-7350

Generic Name
Sodium Phosphate, Monobasic, Monohydrate And Sodium Phosphat...
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
ANDA
Active Listing

Amerisource Bergen

NDC Product
Human Otc Drug

First Aid Antiseptic
NDC 46122-808

Generic Name
First Aid Antiseptic
Dosage Form
Solution
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

AmerisourceBergen Drug Corp

NDC Product
Human Otc Drug

Olopatadine Hydrochloride
NDC 46122-823

Generic Name
Olopatadine Hydrochloride Ophthalmic
Dosage Form
Solution
Route
Ophthalmic
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Olopatadine Hydrochloride
NDC 46122-824

Generic Name
Olopatadine Hydrochloride
Dosage Form
Solution
Route
Ophthalmic
Marketing
ANDA
Active Listing

Aquestive Therapeutics

NDC Product
Human Prescription Drug

Sympazan
NDC 10094-205

Generic Name
Clobazam
Dosage Form
Film
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Sympazan
NDC 10094-210

Generic Name
Clobazam
Dosage Form
Film
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Sympazan
NDC 10094-220

Generic Name
Clobazam
Dosage Form
Film
Route
Oral
Marketing
NDA
Active Listing

AstraZeneca Pharmaceuticals LP

NDC Product
Human Prescription Drug

Wainua
NDC 0310-9400

Generic Name
Eplontersen
Dosage Form
Injection, Solution
Route
Subcutaneous
Marketing
NDA
Active Listing

Bausch & Lomb Incorporated

NDC Product
Human Prescription Drug

Latanoprost
NDC 24208-463

Generic Name
Latanoprost
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Xiidra
NDC 24208-911

Generic Name
Lifitegrast
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
NDA
Active Listing

Baxter Healthcare Corporation

NDC Product
Human Prescription Drug

Myxredlin
NDC 0338-0126

Generic Name
Insulin Human
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
BLA
Active Listing
NDC Product
Human Prescription Drug

Daptomycin In Sodium Chloride
NDC 0338-0712

Generic Name
Daptomycin In Sodium Chloride
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Daptomycin In Sodium Chloride
NDC 0338-0714

Generic Name
Daptomycin In Sodium Chloride
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Daptomycin In Sodium Chloride
NDC 0338-0716

Generic Name
Daptomycin In Sodium Chloride
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Daptomycin In Sodium Chloride
NDC 0338-0718

Generic Name
Daptomycin In Sodium Chloride
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
NDA
Active Listing

Beach Products, Inc.

NDC Product
Human Prescription Drug

K Phos Neutral
NDC 0486-1125

Generic Name
Sodium Phosphate, Dibasic, Anhydrous, Potassium Phosphate, M...
Dosage Form
Tablet, Coated
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Better Living Brands, LLC

NDC Product
Human Otc Drug

First Aid Antiseptic
NDC 21130-891

Generic Name
Povidone-iodine
Dosage Form
Solution
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Bioelements, Inc.

NDC Product
Human Otc Drug

Daily Meds
NDC 49825-100

Generic Name
Salicylic Acid
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

CLINIQUE LABORATORIES LLC

Camber Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Enalapril Maleate Oral Solution
NDC 31722-020

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

Nimodipine
NDC 31722-039

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

Omeprazole
NDC 31722-527

Generic Name
Omeprazole
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Omeprazole
NDC 31722-528

Generic Name
Omeprazole
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Clobazam
NDC 31722-641

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

Spironolactone
NDC 31722-691

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

Chattem, Inc.

NDC Product
Human Otc Drug

Act Anticavity Fluoride Cinnamon
NDC 41167-0940

Generic Name
Sodium Fluoride
Dosage Form
Rinse
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Act Kids Berry Blast
NDC 41167-0976

Generic Name
Sodium Fluoride
Dosage Form
Rinse
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Act Whitening Anticavity Gentle Mint
NDC 41167-0983

Generic Name
Sodium Fluoride 0.02 (0.009 W/v Fluoride Ion)
Dosage Form
Mouthwash
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Church & Dwight Co., Inc.

NDC Product
Human Otc Drug

Zicam Extreme Congestion Relief
NDC 10237-464

Generic Name
Oxymetazoline Hydrochloride
Dosage Form
Spray
Route
Nasal
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Zicam Intense Sinus Relief
NDC 10237-471

Generic Name
Oxymetazoline Hydrochloride
Dosage Form
Spray
Route
Nasal
Marketing
OTC MONOGRAPH DRUG
Active Listing

Colgate-Palmolive - do not use

NDC Product
Human Otc Drug

Colgate Enamel Strength Mouthwash
NDC 35000-734

Generic Name
Sodium Fluoride
Dosage Form
Rinse
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing

Colgate-Palmolive Company

NDC Product
Human Otc Drug

Colgate Kids Minions Mouthwash
NDC 35000-727

Generic Name
Sodium Fluoride
Dosage Form
Rinse
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing

Cosette Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Hydrocortisone Valerate
NDC 0713-0560

Generic Name
Hydrocortisone Valerate
Dosage Form
Ointment
Route
Topical
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Hydrocortisone Valerate
NDC 0713-0720

Generic Name
Hydrocortisone Valerate
Dosage Form
Cream
Route
Topical
Marketing
ANDA
Active Listing

Dr. Reddy's Laboratories Inc

NDC Product
Human Prescription Drug

Methylprednisolone Sodium Succinate
NDC 43598-127

Generic Name
Methylprednisolone Sodium Succinate
Dosage Form
Injection
Route
Intramuscular; Intravenous
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Methylprednisolone Sodium Succinate
NDC 43598-128

Generic Name
Methylprednisolone Sodium Succinate
Dosage Form
Injection
Route
Intramuscular; Intravenous
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Methylprednisolone Sodium Succinate
NDC 43598-129

Generic Name
Methylprednisolone Sodium Succinate
Dosage Form
Injection
Route
Intramuscular; Intravenous
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Methylprednisolone Sodium Succinate
NDC 43598-130

Generic Name
Methylprednisolone Sodium Succinate
Dosage Form
Injection
Route
Intramuscular; Intravenous
Marketing
ANDA
Active Listing

Dr. Reddy's Laboratories Inc.

NDC Product
Bulk Ingredient

NDC 43598-764

Generic Name
Olopatadine Hydrochloride Ophthalmic
Dosage Form
Solution
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing

Dr.Reddys Laboratories Inc

NDC Product
Human Prescription Drug

Buprenorphine And Naloxone
NDC 43598-579

Generic Name
Buprenorphine And Naloxone
Dosage Form
Film, Soluble
Route
Buccal; Sublingual
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Buprenorphine And Naloxone
NDC 43598-580

Generic Name
Buprenorphine And Naloxone
Dosage Form
Film, Soluble
Route
Buccal; Sublingual
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Buprenorphine And Naloxone
NDC 43598-581

Generic Name
Buprenorphine And Naloxone
Dosage Form
Film, Soluble
Route
Buccal; Sublingual
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Buprenorphine And Naloxone
NDC 43598-582

Generic Name
Buprenorphine And Naloxone
Dosage Form
Film, Soluble
Route
Buccal; Sublingual
Marketing
ANDA
Active Listing

E.R. Squibb & Sons, L.L.C.

NDC Product
Human Prescription Drug

Orencia
NDC 0003-2188

Generic Name
Abatacept
Dosage Form
Injection, Solution
Route
Subcutaneous
Marketing
BLA
Active Listing
NDC Product
Human Prescription Drug

Orencia
NDC 0003-2814

Generic Name
Abatacept
Dosage Form
Injection, Solution
Route
Subcutaneous
Marketing
BLA
Active Listing
NDC Product
Human Prescription Drug

Orencia
NDC 0003-2818

Generic Name
Abatacept
Dosage Form
Injection, Solution
Route
Subcutaneous
Marketing
BLA
Active Listing

EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)

NDC Product
Human Otc Drug

Childrens Allergy
NDC 49035-208

Generic Name
Fexofenadine Hcl
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

Genentech, Inc.

NDC Product
Human Prescription Drug

Avastin
NDC 50242-060

Generic Name
Bevacizumab
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
BLA
Active Listing
NDC Product
Human Prescription Drug

Avastin
NDC 50242-061

Generic Name
Bevacizumab
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
BLA
Active Listing

Genomma Lab USA

NDC Product
Human Otc Drug

Tukol Max Action
NDC 50066-518

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

H E B

NDC Product
Human Otc Drug

Once Daily Relief
NDC 37808-045

Generic Name
Olopatadine Hydrochloride Ophthalmic Solution
Dosage Form
Solution
Route
Ophthalmic
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Anticavity
NDC 37808-119

Generic Name
Sodium Fluoride
Dosage Form
Rinse
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Anticavity Fluoride Rinse
NDC 37808-163

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Anticavity Fluoride Rinse
NDC 37808-213

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Anticavity
NDC 37808-435

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Alcohol Free Refreshing Mint
NDC 37808-576

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Children Allergy
NDC 37808-654

Generic Name
Fexofenadine Hcl
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Anticavity Rinse
NDC 37808-808

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Alcohol-free Anticavity
NDC 37808-942

Generic Name
Sodium Fluoride
Dosage Form
Liquid
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

HART Health

NDC Product
Human Otc Drug

Povidone-iodine
NDC 50332-0056

Generic Name
Povidone-iodine
Dosage Form
Solution
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Haleon US Holdings LLC

Henry Schein, Inc.

NDC Product
Human Prescription Drug

Digoxin
NDC 0404-9850

Generic Name
Digoxin
Dosage Form
Injection
Route
Intramuscular; Intravenous
Marketing
ANDA
Active Listing

Hikma Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Digoxin
NDC 0641-1410

Generic Name
Digoxin
Dosage Form
Injection
Route
Intramuscular; Intravenous
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Digoxin
NDC 0641-6184

Generic Name
Digoxin
Dosage Form
Injection
Route
Intramuscular; Intravenous
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Sodium Tetradecyl Sulfate
NDC 24201-201

Generic Name
Sodium Tetradecyl Sulfate
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
ANDA
Active Listing

Honeywell Safety Products, Inc.

NDC Product
Human Otc Drug

Eyesaline Eyewash Concentrate
NDC 0498-2501

Generic Name
Purified Water
Dosage Form
Liquid
Route
Ophthalmic
Marketing
OTC MONOGRAPH DRUG
Active Listing

Hospira, Inc.

NDC Product
Human Prescription Drug

Regadenoson
NDC 0409-1401

Generic Name
Regadenoson
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Sodium Phosphates
NDC 0409-7391

Generic Name
Sodium Phosphate, Monobasic, Monohydrate And Sodium Phosphat...
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
NDA
Active Listing

Janssen Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Invega Sustenna
NDC 50458-560

Generic Name
Paliperidone Palmitate
Dosage Form
Injection
Route
Intramuscular
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Invega Sustenna
NDC 50458-561

Generic Name
Paliperidone Palmitate
Dosage Form
Injection
Route
Intramuscular
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Invega Sustenna
NDC 50458-562

Generic Name
Paliperidone Palmitate
Dosage Form
Injection
Route
Intramuscular
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Invega Sustenna
NDC 50458-563

Generic Name
Paliperidone Palmitate
Dosage Form
Injection
Route
Intramuscular
Marketing
NDA
Active Listing

KROGER COMPANY

L'Oreal USA Products Inc

Lannett Company, Inc.

NDC Product
Human Prescription Drug

Sumatriptan
NDC 0527-1818

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

Sumatriptan
NDC 0527-1859

Generic Name
Sumatriptan
Dosage Form
Spray
Route
Nasal
Marketing
ANDA
Active Listing

Lupin Pharmaceuticals,Inc.

L�Oreal USA Products Inc

Major Pharmaceuticals

NDC Product
Human Otc Drug

Major Nasal Decongestant
NDC 0904-7435

Generic Name
Oxymetazoline Hydrochloride
Dosage Form
Spray
Route
Nasal
Marketing
OTC MONOGRAPH DRUG
Active Listing

Meijer Distribution, Inc.

NDC Product
Human Otc Drug

Meijer Dry Eye Relief
NDC 41250-718

Generic Name
Glycerin, Hypromellose, Polyethylene Glycol 400
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Meijer Artificial Tears
NDC 41250-819

Generic Name
Polyvinyl Alcohol, Povidone
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
OTC MONOGRAPH DRUG
Active Listing

Meijer, Inc.

NDC Product
Human Otc Drug

Anticavity
NDC 41250-163

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Anticavity Fluoride Rinse
NDC 41250-213

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Alcohol-free Anticavity
NDC 41250-482

Generic Name
Sodium Fluoride
Dosage Form
Liquid
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Oral Antivavity
NDC 41250-576

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Anticavity
NDC 41250-581

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

First Aid Antiseptic
NDC 41250-720

Generic Name
Povidone-iodine
Dosage Form
Solution
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Anticavity
NDC 41250-971

Generic Name
Sodium Fluoride
Dosage Form
Rinse
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Micro Labs Limited

NDC Product
Human Prescription Drug

Latanoprost
NDC 42571-499

Generic Name
Latanoprost
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
ANDA
Active Listing

NCS HealthCare of KY, LLC dba Vangard Labs

NDC Product
Human Prescription Drug

Omeprazole
NDC 0615-8406

Generic Name
Omeprazole
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Nice-Pak Products, LLC

NorthStar RxLLC

NDC Product
Human Prescription Drug

Clobazam
NDC 16714-087

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

Novartis Pharmaceuticals Corporation

NDC Product
Human Prescription Drug

Simulect
NDC 0078-0331

Generic Name
Basiliximab
Dosage Form
Injection, Powder, For Solution
Route
Intravenous
Marketing
BLA
Active Listing
NDC Product
Human Prescription Drug

Simulect
NDC 0078-0393

Generic Name
Basiliximab
Dosage Form
Injection, Powder, For Solution
Route
Intravenous
Marketing
BLA
Active Listing
NDC Product
Human Prescription Drug

Xiidra
NDC 0078-0911

Generic Name
Lifitegrast
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
NDA
Active Listing

PAI Holdings, LLC dba PAI Pharma

NDC Product
Human Prescription Drug

Cimetidine Hydrochloride
NDC 0121-1025

Generic Name
Cimetidine Hydrochloride
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

Padagis Israel Pharmaceuticals Ltd

NDC Product
Human Prescription Drug

Sumatriptan
NDC 45802-598

Generic Name
Sumatriptan
Dosage Form
Spray
Route
Nasal
Marketing
ANDA
Active Listing

Patrin Pharma, Inc.

NDC Product
Human Prescription Drug

Pregabalin
NDC 39328-090

Generic Name
Pregabalin
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

Pfizer Laboratories Div Pfizer Inc

NDC Product
Human Prescription Drug

Retacrit
NDC 0069-1305

Generic Name
Epoetin Alfa-epbx
Dosage Form
Injection, Solution
Route
Intravenous; Subcutaneous
Marketing
BLA
Active Listing
NDC Product
Human Prescription Drug

Retacrit
NDC 0069-1306

Generic Name
Epoetin Alfa-epbx
Dosage Form
Injection, Solution
Route
Intravenous; Subcutaneous
Marketing
BLA
Active Listing
NDC Product
Human Prescription Drug

Retacrit
NDC 0069-1307

Generic Name
Epoetin Alfa-epbx
Dosage Form
Injection, Solution
Route
Intravenous; Subcutaneous
Marketing
BLA
Active Listing
NDC Product
Human Prescription Drug

Retacrit
NDC 0069-1308

Generic Name
Epoetin Alfa-epbx
Dosage Form
Injection, Solution
Route
Intravenous; Subcutaneous
Marketing
BLA
Active Listing
NDC Product
Human Prescription Drug

Retacrit
NDC 0069-1309

Generic Name
Epoetin Alfa-epbx
Dosage Form
Injection, Solution
Route
Intravenous; Subcutaneous
Marketing
BLA
Active Listing
NDC Product
Human Prescription Drug

Retacrit
NDC 0069-1311

Generic Name
Epoetin Alfa-epbx
Dosage Form
Injection, Solution
Route
Intravenous; Subcutaneous
Marketing
BLA
Active Listing
NDC Product
Human Prescription Drug

Retacrit
NDC 0069-1318

Generic Name
Epoetin Alfa-epbx
Dosage Form
Injection, Solution
Route
Intravenous; Subcutaneous
Marketing
BLA
Active Listing

Pharmacia & Upjohn Company LLC

NDC Product
Human Prescription Drug

Depo-subq Provera
NDC 0009-4709

Generic Name
Medroxyprogesterone Acetate
Dosage Form
Injection, Suspension
Route
Subcutaneous
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Somavert
NDC 0009-7166

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

Somavert
NDC 0009-7168

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

Somavert
NDC 0009-7188

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

Somavert
NDC 0009-7199

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

Somavert
NDC 0009-7200

Generic Name
Pegvisomant
Dosage Form
Kit
Route
N/A
Marketing
BLA
Active Listing

Rising Pharma Holdings, Inc.

NDC Product
Human Otc Drug

Olopatadine Hydrochloride
NDC 16571-861

Generic Name
Olopatadine Hydrochloride
Dosage Form
Solution
Route
Ophthalmic
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Olopatadine Hydrochloride
NDC 16571-882

Generic Name
Olopatadine Hydrochloride
Dosage Form
Solution
Route
Ophthalmic
Marketing
ANDA
Active Listing

Rite Aid Corporation

NDC Product
Human Otc Drug

Anticavity Rinse
NDC 11822-4004

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

First Aid Antiseptic
NDC 11822-9050

Generic Name
Povidone-iodine
Dosage Form
Solution
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Anticavity
NDC 11822-9718

Generic Name
Sodium Fluoride
Dosage Form
Rinse
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Rugby Laboratories

NDC Product
Human Otc Drug

Olopatadine Hydrochloride
NDC 0536-1307

Generic Name
Olopatadine Hydrochloride
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
ANDA
Active Listing

Sagent Pharmaceuticals

NDC Product
Human Prescription Drug

Latanoprost
NDC 25021-001

Generic Name
Latanoprost
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Vecuronium Bromide
NDC 25021-685

Generic Name
Vecuronium Bromide
Dosage Form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Vecuronium Bromide
NDC 25021-686

Generic Name
Vecuronium Bromide
Dosage Form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing
ANDA
Active Listing

Sandoz Inc.

NDC Product
Human Prescription Drug

Methylprednisolone Acetate
NDC 0781-3516

Generic Name
Methylprednisolone Acetate
Dosage Form
Injection, Suspension
Route
Intralesional; Intramuscular; Intrasynovial; Soft Tissue
Marketing
ANDA
Active Listing

Sheffield Pharmaceuticals LLC

Sun Pharmaceutical Industries, Inc.

NDC Product
Human Prescription Drug

Cequa
NDC 47335-506

Generic Name
Cyclosporine
Dosage Form
Solution/ Drops
Route
Ophthalmic; Topical
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Cequa
NDC 47335-507

Generic Name
Cyclosporine
Dosage Form
Solution/ Drops
Route
Ophthalmic; Topical
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Vecuronium Bromide
NDC 47335-931

Generic Name
Vecuronium Bromide
Dosage Form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Vecuronium Bromide
NDC 47335-932

Generic Name
Vecuronium Bromide
Dosage Form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing
ANDA
Active Listing

Target Corporation

NDC Product
Human Otc Drug

First Aid Antiseptic
NDC 11673-003

Generic Name
Povidone-iodine
Dosage Form
Solution
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Anticavity
NDC 11673-004

Generic Name
Sodium Fluoride
Dosage Form
Rinse
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Anticavity Fluoride Rinse
NDC 11673-163

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Fluoride Mouth Rinse Anticavity
NDC 11673-213

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

The Kroger Co.

NDC Product
Human Otc Drug

Anticavity
NDC 30142-004

Generic Name
Sodium Fluoride
Dosage Form
Rinse
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Anticavity
NDC 30142-163

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Alcohol-free Anticavity
NDC 30142-482

Generic Name
Sodium Fluoride
Dosage Form
Liquid
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Oral Antivavity
NDC 30142-576

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

The Procter & Gamble Manufacturing Company

NDC Product
Human Otc Drug

Kids Crest Bubblegum Rush
NDC 37000-167

Generic Name
Sodium Fluoride
Dosage Form
Rinse
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Crest Complete Plus 3 In 1
NDC 37000-984

Generic Name
Sodium Fluoride
Dosage Form
Gel, Dentifrice
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing

Topco Associates LLC

NDC Product
Human Otc Drug

First Aid Antiseptic
NDC 36800-011

Generic Name
Povidone-iodine
Dosage Form
Solution
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Alcohol-free Anticavity
NDC 36800-482

Generic Name
Sodium Fluoride
Dosage Form
Liquid
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Anticavity
NDC 36800-803

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Anticavity
NDC 36800-971

Generic Name
Sodium Fluoride
Dosage Form
Rinse
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

United Natural Foods, Inc. dba UNFI

NDC Product
Human Otc Drug

Anticavity
NDC 41163-011

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Anticavity
NDC 41163-581

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Anticavity
NDC 41163-971

Generic Name
Sodium Fluoride
Dosage Form
Rinse
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Upsher-Smith Laboratories, LLC

NDC Product
Human Prescription Drug

Tosymra
NDC 0245-0812

Generic Name
Sumatriptan
Dosage Form
Spray
Route
Nasal
Marketing
NDA
Active Listing

WALGREEN COMPANY

WALGREENS CO.

NDC Product
Human Otc Drug

Walgreens Senna Laxative
NDC 0363-7120

Generic Name
Sennosides
Dosage Form
Liquid
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Wal-Mart Stores,Inc.,

Walgreen Co.

NDC Product
Human Otc Drug

Anticavity
NDC 0363-0171

Generic Name
Sodium Fluoride
Dosage Form
Rinse
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

First Aid Antiseptic
NDC 0363-0777

Generic Name
Povidone-iodine
Dosage Form
Solution
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Walgreen Company

NDC Product
Human Otc Drug

First Aid Antiseptic
NDC 0363-6280

Generic Name
Povidone-iodine 5%
Dosage Form
Spray
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Walgreens Company

Walmart Inc.

NDC Product
Human Otc Drug

Anticavity Rinse
NDC 49035-004

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

First Aid Antiseptic
NDC 49035-050

Generic Name
Povidone-iodine
Dosage Form
Solution
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Anticavity
NDC 49035-581

Generic Name
Sodium Fluoride
Dosage Form
Mouthwash
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Anticavity
NDC 49035-971

Generic Name
Sodium Fluoride
Dosage Form
Rinse
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

External Clinical & Regulatory Resources

CAS
Common Chemistry
NCATS
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NLM
DailyMed Products
NCATS
GSRS Full Record
NIH
NCI Thesaurus
NLM
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