D&C RED NO. 28
UNII 767IP0Y5NH

Substance Identification & Data

This profile provides standardized clinical and technical data for D&c Red No. 28, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 767IP0Y5NH.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 18472-87-2 and the RxNorm Concept ID (RxCUI) 1310707. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
767IP0Y5NH
CAS Registry Number
18472-87-2
RxNorm Concept ID
1310707

Detailed Substance Profile

Preferred Name
D&C RED NO. 28
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
767IP0Y5NH
The specific atomic composition represented as a molecular structure string.
InChIKey
C20H2Br4Cl4O5.2Na
International Chemical Identifier digital signature for unique molecular identification.
SMILES String
GVKCHTBDSMQENH-UHFFFAOYSA-L
Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
C71660
National Cancer Institute reference terminology for clinical and research data.
PubChem CID
2724057
Unique identification number in the NCBI database of chemical substances.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
c1(c(Br)cc2c(oc3-c(c2-c4c(c(c(c(c4C([O-])=O)Cl)Cl)Cl)Cl)cc(c(=O)c3Br)Br)c1Br)[O-].[Na+].[Na+]

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for D&c Red No. 28. 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

ACID RED 92
AKA104(1)
CI 45410
RED 28

Common Names & Synonyms

2,4,5,7-TETRABROMO-4,5,6,7-TETRACHLOROFLUORESCEIN DISODIUM SALT
C.I. 45410
C.I. ACID RED 92
CYANOSIN
D & C RED #28 [VANDF]
D & C RED NO. 28
D&C RED NO. 27 DISODIUM SALT
D&C RED NO. 28
D&C RED NO. 28 [II]
DC RED NO. 28
EOSIN BLUE
FD&C RED NO. 28 (DELISTED)
FD&C RED NO. 28 (DELISTED) [II]
JAPAN RED 104
PHLOXIN B
PHLOXINE B
PHLOXINE B [MI]
RED NO. 104

Systematic Nomenclature

FLUORESCEIN, 2',4',5',7'-TETRABROMO-4,5,6,7-TETRACHLORO-, DISODIUM SALT
SPIRO(ISOBENZOFURAN-1(3H),9'-(9H)XANTHEN)-3-ONE, 2',4',5',7'-TETRABROMO-4,5,6,7-TETRACHLORO-3',6'-DIHYDROXY-, DISODIUM SALT
SPIRO(ISOBENZOFURAN-1(3H),9'-(9H)XANTHEN)-3-ONE, 2',4',5',7'-TETRABROMO-4,5,6,7-TETRACHLORO-3',6'-DIHYDROXY-, SODIUM SALT (1:2)

Technical Codes

NSC-10462

NDC Products Containing D&C RED NO. 28

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.
→ AbbVie Inc. 1
→ Accord Healthcare, Inc. 2
→ Actavis Pharma, Inc. 18
→ Amneal Pharmaceuticals of New York LLC 20
→ AstraZeneca Pharmaceuticals LP 7
→ Bausch Health US, LLC 6
→ Bayer HealthCare LLC. 1
→ Calvin Scott & Co., Inc. 1
→ ESTEE LAUDER INC 1
→ Endo USA, Inc. 2
→ Haleon US Holdings LLC 2
→ Henry Schein Inc. 8
→ Hikma Pharmaceuticals USA Inc. 5
→ KVK-Tech, Inc. 1
→ Kao USA Inc. 1
→ L. Perrigo Company 2
→ Lannett Company, Inc. 12
→ Major Pharmaceuticals 5
→ Marlex Pharmaceuticals Inc 2
→ Mylan Pharmaceuticals Inc. 5
→ NCS HealthCare of KY, LLC dba Vangard Labs 3
→ NORTHSTAR RX LLC 3
→ NorthStar Rx LLC 6
→ Northstar Rx LLC 5
→ Northstar Rx LLC. 3
→ Patriot Pharmaceuticals 1
→ Pharbest Pharmaceuticals, Inc. 2
→ REVLON 1
→ RITE AID CORPORATION 3
→ Rising Pharma Holdings, Inc. 1
→ Rite Aid Corporation 2
→ Rugby Laboratories, Inc 1
→ Rugby Laboratories, Inc. 2
→ SUNRISE PHARMACEUTICAL, INC. 1
→ SpecGx LLC 6
→ TARGET CORPORATION 2
→ TARGET Corporation 2
→ Target Corporation 3
→ Teva Pharmaceuticals USA, Inc. 28
→ Teva Pharmaceuticals, Inc. 7
→ Torrent Pharmaceuticals Limited 1
→ WALGREEN CO. 1
→ WALGREEN COMPANY 2
→ WALGREENS CO. 3
→ Walgreen Company 4
→ Walgreens 4
→ Walgreens company 1

AbbVie Inc.

NDC Product
Human Prescription Drug

Depakote Sprinkles
NDC 0074-6114

Generic Name
Divalproex Sodium
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing

Accord Healthcare, Inc.

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 16729-304

Generic Name
Diltiazem Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 16729-305

Generic Name
Diltiazem Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Actavis Pharma, Inc.

NDC Product
Drug For Further Processing

NDC 0228-2067

Generic Name
Oxazepam
Dosage Form
Capsule, Gelatin Coated
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Oxazepam
NDC 0228-2067

Generic Name
Oxazepam
Dosage Form
Capsule, Gelatin Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxazepam
NDC 0228-2069

Generic Name
Oxazepam
Dosage Form
Capsule, Gelatin Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0228-2069

Generic Name
Oxazepam
Dosage Form
Capsule, Gelatin Coated
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing

NDC 0228-2073

Generic Name
Oxazepam
Dosage Form
Capsule, Gelatin Coated
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Oxazepam
NDC 0228-2073

Generic Name
Oxazepam
Dosage Form
Capsule, Gelatin Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Hydrochlorothiazide
NDC 0591-0347

Generic Name
Hydrochlorothiazide
Dosage Form
Capsule, Gelatin Coated
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Drug For Further Processing

NDC 0591-0347

Generic Name
Hydrochlorothiazide
Dosage Form
Capsule, Gelatin Coated
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Dicyclomine Hydrochloride
NDC 0591-0794

Generic Name
Dicyclomine Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0591-0794

Generic Name
Dicyclomine Hydrochloride
Dosage Form
Capsule
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing

NDC 0591-0795

Generic Name
Dicyclomine Hydrochloride
Dosage Form
Tablet
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Dicyclomine Hydrochloride
NDC 0591-0795

Generic Name
Dicyclomine Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0591-3153

Generic Name
Minocycline Hydrochloride
Dosage Form
Capsule
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Trospium Chloride
NDC 0591-3636

Generic Name
Trospium Chloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Minocycline Hydrochloride
NDC 0591-5694

Generic Name
Minocycline Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0591-5694

Generic Name
Minocycline Hydrochloride
Dosage Form
Capsule
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing

NDC 0591-5695

Generic Name
Minocycline Hydrochloride
Dosage Form
Capsule
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Minocycline Hydrochloride
NDC 0591-5695

Generic Name
Minocycline Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

Amneal Pharmaceuticals of New York LLC

NDC Product
Human Prescription Drug

Carvedilol Phosphate
NDC 0115-1249

Generic Name
Carvedilol Phosphate
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Carvedilol Phosphate
NDC 0115-1250

Generic Name
Carvedilol Phosphate
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Carvedilol Phosphate
NDC 0115-1251

Generic Name
Carvedilol Phosphate
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate
NDC 0115-1281

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

Morphine Sulfate
NDC 0115-1282

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

Morphine Sulfate
NDC 0115-1479

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

Dexmethylphenidate Hydrochloride
NDC 0115-1682

Generic Name
Dexmethylphenidate Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dexmethylphenidate Hydrochloride
NDC 0115-1683

Generic Name
Dexmethylphenidate Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dexmethylphenidate Hydrochloride
NDC 0115-1684

Generic Name
Dexmethylphenidate Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dexmethylphenidate Hydrochloride
NDC 0115-1685

Generic Name
Dexmethylphenidate Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Methylphenidate Hydrochloride
NDC 0115-1737

Generic Name
Methylphenidate Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Methylphenidate Hydrochloride
NDC 0115-1738

Generic Name
Methylphenidate Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Methylphenidate Hydrochloride
NDC 0115-1739

Generic Name
Methylphenidate Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Methylphenidate Hydrochloride
NDC 0115-1740

Generic Name
Methylphenidate Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Methylphenidate Hydrochloride
NDC 0115-1741

Generic Name
Methylphenidate Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tamsulosin Hydrochloride
NDC 0115-8211

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

Dexmethylphenidate Hydrochloride
NDC 0115-9918

Generic Name
Dexmethylphenidate Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dexmethylphenidate Hydrochloride
NDC 0115-9919

Generic Name
Dexmethylphenidate Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dexmethylphenidate Hydrochloride
NDC 0115-9920

Generic Name
Dexmethylphenidate Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dexmethylphenidate Hydrochloride
NDC 0115-9921

Generic Name
Dexmethylphenidate Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

AstraZeneca Pharmaceuticals LP

NDC Product
Human Prescription Drug

Nexium
NDC 0186-4010

Generic Name
Esomeprazole Magnesium
Dosage Form
Granule, Delayed Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Nexium
NDC 0186-4020

Generic Name
Esomeprazole Magnesium
Dosage Form
Granule, Delayed Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Nexium
NDC 0186-4025

Generic Name
Esomeprazole Magnesium
Dosage Form
Granule, Delayed Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Nexium
NDC 0186-4040

Generic Name
Esomeprazole Magnesium
Dosage Form
Granule, Delayed Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Nexium
NDC 0186-4050

Generic Name
Esomeprazole Magnesium
Dosage Form
Granule, Delayed Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Nexium
NDC 0186-5020

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Nexium
NDC 0186-5040

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
NDA
Active Listing

Bausch Health US, LLC

NDC Product
Human Prescription Drug

Tiazac Extended Release
NDC 0187-2612

Generic Name
Diltiazem Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Tiazac Extended Release
NDC 0187-2613

Generic Name
Diltiazem Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Tiazac Extended Release
NDC 0187-2614

Generic Name
Diltiazem Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Tiazac Extended Release
NDC 0187-2615

Generic Name
Diltiazem Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Tiazac Extended Release
NDC 0187-2616

Generic Name
Diltiazem Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Tiazac Extended Release
NDC 0187-2617

Generic Name
Diltiazem Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA
Active Listing

Bayer HealthCare LLC.

NDC Product
Human Otc Drug

Phillips Milk Of Magnesia Wild Cherry
NDC 0280-0032

Generic Name
Phillips Milk Of Magnesia Wild Cherry
Dosage Form
Liquid
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Calvin Scott & Co., Inc.

NDC Product
Human Prescription Drug

Phentermine Hydrochloride
NDC 17224-877

Generic Name
Phentermine Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

ESTEE LAUDER INC

Endo USA, Inc.

NDC Product
Human Prescription Drug

Fluvoxamine Maleate
NDC 10370-175

Generic Name
Fluvoxamine Maleate
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fluvoxamine Maleate
NDC 10370-176

Generic Name
Fluvoxamine Maleate
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Haleon US Holdings LLC

NDC Product
Human Otc Drug

Nexium 24hr
NDC 0573-2450

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

Nexium 24hr Clearminis
NDC 0573-2452

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
NDA
Active Listing

Henry Schein Inc.

NDC Product
Human Otc Drug

Benzo-jel
NDC 0404-0032

Generic Name
Benzocaine
Dosage Form
Gel
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Benzo-jel
NDC 0404-0033

Generic Name
Benzocaine
Dosage Form
Gel
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Benzo-jel
NDC 0404-0034

Generic Name
Benzocaine
Dosage Form
Gel
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Benzo-jel
NDC 0404-0035

Generic Name
Benzocaine
Dosage Form
Gel
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Benzo-jel
NDC 0404-0036

Generic Name
Benzocaine
Dosage Form
Gel
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Benzo-jel
NDC 0404-0037

Generic Name
Benzocaine
Dosage Form
Gel
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Benzo-jel
NDC 0404-0038

Generic Name
Benzocaine
Dosage Form
Gel
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Benzo-jel
NDC 0404-0039

Generic Name
Benzocaine
Dosage Form
Gel
Route
Dental
Marketing
OTC MONOGRAPH DRUG
Active Listing

Hikma Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Ramipril
NDC 0054-0108

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

Ramipril
NDC 0054-0109

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

Lisdexamfetamine Dimesylate
NDC 0054-0373

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

Lisdexamfetamine Dimesylate
NDC 0054-0374

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

Lisdexamfetamine Dimesylate
NDC 0054-0375

Generic Name
Lisdexamfetamine Dimesylate
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

KVK-Tech, Inc.

NDC Product
Human Prescription Drug

Phentermine Hydrochloride
NDC 10702-028

Generic Name
Phentermine Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

Kao USA Inc.

L. Perrigo Company

NDC Product
Human Otc Drug

Good Sense Lansoprazole
NDC 0113-1114

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

Prevacid 24 Hr
NDC 0113-6117

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

Lannett Company, Inc.

NDC Product
Human Prescription Drug

Danazol
NDC 0527-1369

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

Loxapine
NDC 0527-1395

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

Loxapine
NDC 0527-1396

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

Loxapine
NDC 0527-1397

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

Major Pharmaceuticals

NDC Product
Human Prescription Drug

Ursodiol
NDC 0904-6221

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

Divalproex Sodium
NDC 0904-6615

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

Prazosin Hydrochloride
NDC 0904-7021

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

Prazosin Hydrochloride
NDC 0904-7022

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

Rifampin
NDC 0904-7315

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

Marlex Pharmaceuticals Inc

NDC Product
Human Prescription Drug

Prazosin Hydrochloride
NDC 10135-667

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

Prazosin Hydrochloride
NDC 10135-668

Generic Name
Prazosin Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

Mylan Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Tacrolimus
NDC 0378-2045

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

Tacrolimus
NDC 0378-2046

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

Tacrolimus
NDC 0378-2047

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

Prazosin Hydrochloride
NDC 0378-2302

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

Prazosin Hydrochloride
NDC 0378-3205

Generic Name
Prazosin Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

NCS HealthCare of KY, LLC dba Vangard Labs

NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 0615-8237

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

Prazosin Hydrochloride
NDC 0615-8520

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

Calcium Acetate
NDC 0615-8632

Generic Name
Calcium Acetate
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

NORTHSTAR RX LLC

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 16714-523

Generic Name
Diltiazem Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 16714-524

Generic Name
Diltiazem Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 16714-525

Generic Name
Diltiazem Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

NorthStar Rx LLC

NDC Product
Human Prescription Drug

Omeprazole
NDC 16714-123

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

Amoxicillin
NDC 16714-298

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

Amoxicillin
NDC 16714-299

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

Cefadroxil
NDC 16714-388

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

Omeprazole
NDC 16714-714

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

Omeprazole
NDC 16714-715

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

Northstar Rx LLC

NDC Product
Human Prescription Drug

Atomoxetine
NDC 16714-757

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

Atomoxetine
NDC 16714-758

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

Atomoxetine
NDC 16714-759

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

Atomoxetine
NDC 16714-760

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

Atomoxetine
NDC 16714-761

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

Northstar Rx LLC.

NDC Product
Human Prescription Drug

Clomipramine Hydrochloride
NDC 16714-849

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

Clomipramine Hydrochloride
NDC 16714-850

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

Clomipramine Hydrochloride
NDC 16714-851

Generic Name
Clomipramine Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

Patriot Pharmaceuticals

NDC Product
Human Prescription Drug

Itraconazole
NDC 10147-1700

Generic Name
Itraconazole
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing

Pharbest Pharmaceuticals, Inc.

NDC Product
Human Otc Drug

Pharbedryl
NDC 16103-347

Generic Name
Diphenhydramine Hcl
Dosage Form
Capsule
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Pharbedryl
NDC 16103-348

Generic Name
Diphenhydramine Hcl
Dosage Form
Capsule
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

REVLON

NDC Product
Human Otc Drug

Ea Eight Hr Lip Sheer Tints
NDC 10967-674

Generic Name
Oxybenzone, Padimate O, Petrolatum
Dosage Form
Lipstick
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

RITE AID CORPORATION

NDC Product
Human Otc Drug

Rite Aid Ultra Strnght Pink Bismuth
NDC 11822-7070

Generic Name
Bismuth Subsalicylate
Dosage Form
Suspension
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Rising Pharma Holdings, Inc.

NDC Product
Human Prescription Drug

Calcium Acetate
NDC 16571-813

Generic Name
Calcium Acetate
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

Rite Aid Corporation

NDC Product
Human Otc Drug

Lansoprazole
NDC 11822-0019

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

Allergy Relief
NDC 11822-0190

Generic Name
Diphenhydramine Hcl
Dosage Form
Capsule
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Rugby Laboratories, Inc

NDC Product
Human Otc Drug

Lansoprazole
NDC 0536-1368

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

Rugby Laboratories, Inc.

NDC Product
Human Otc Drug

Stomach Relief Regular Strength
NDC 0536-1286

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

Stomach Relief Ultra
NDC 0536-1287

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

SUNRISE PHARMACEUTICAL, INC.

NDC Product
Human Prescription Drug

Phentermine Hydrochloride
NDC 11534-176

Generic Name
Phentermine Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

SpecGx LLC

TARGET CORPORATION

NDC Product
Human Otc Drug

5-symptom Digestive Relief
NDC 11673-291

Generic Name
Bismuth Subsalicylate
Dosage Form
Suspension
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Ultra Strenght Pink Bismuth
NDC 11673-907

Generic Name
Bismuth Subsalicylate
Dosage Form
Suspension
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

TARGET Corporation

NDC Product
Human Otc Drug

Digestive Relief Regular Strength
NDC 11673-372

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

Digestive Relief Regular Strength
NDC 11673-724

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

Target Corporation

NDC Product
Human Otc Drug

Up And Up Lansoprazole
NDC 11673-280

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

Lansoprazole
NDC 11673-324

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

Up And Up Digestive Relief
NDC 11673-706

Generic Name
Bismuth Subsalicylate
Dosage Form
Suspension
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Amoxicillin
NDC 0093-2267

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

Amoxicillin
NDC 0093-2268

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

Amoxicillin
NDC 0093-3107

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

Amoxicillin
NDC 0093-3109

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

Disopyramide Phosphate
NDC 0093-3127

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

Disopyramide Phosphate
NDC 0093-3129

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

Cefdinir
NDC 0093-3160

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

Prazosin Hydrochloride
NDC 0093-4068

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

Prazosin Hydrochloride
NDC 0093-4069

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

Amoxicillin
NDC 0093-4155

Generic Name
Amoxicillin
Dosage Form
Powder, For Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Olanzapine And Fluoxetine
NDC 0093-5507

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

Fluoxetine
NDC 0093-7198

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

Mycophenolate Mofetil
NDC 0093-7334

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

Sunitinib Malate
NDC 0093-8199

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

Sunitinib Malate
NDC 0093-8224

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

Sunitinib Malate
NDC 0093-8229

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

Sunitinib Malate
NDC 0093-8231

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

Mexiletine Hydrochloride
NDC 0093-8739

Generic Name
Mexiletine Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0093-8739

Generic Name
Mexiletine Hydrochloride
Dosage Form
Capsule
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing

NDC 0093-8740

Generic Name
Mexiletine Hydrochloride
Dosage Form
Capsule
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Mexiletine Hydrochloride
NDC 0093-8740

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

Mexiletine Hydrochloride
NDC 0093-8741

Generic Name
Mexiletine Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0093-8741

Generic Name
Mexiletine Hydrochloride
Dosage Form
Capsule
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Hydroxyzine Pamoate
NDC 0555-0302

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

Hydroxyzine Pamoate
NDC 0555-0323

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

Hydroxyzine Pamoate
NDC 0555-0324

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

Danazol
NDC 0555-0635

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

Hydroxyurea
NDC 0555-0882

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

Teva Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Lisdexamfetamine Dimesylate
NDC 0480-3564

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

Lisdexamfetamine Dimesylate
NDC 0480-3565

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

Lisdexamfetamine Dimesylate
NDC 0480-3566

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

Lisdexamfetamine Dimesylate
NDC 0480-3567

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

Lisdexamfetamine Dimesylate
NDC 0480-3568

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

Lisdexamfetamine Dimesylate
NDC 0480-3569

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

Lisdexamfetamine Dimesylate
NDC 0480-3570

Generic Name
Lisdexamfetamine Dimesylate
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

Torrent Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Itraconazole
NDC 13668-463

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

WALGREEN CO.

NDC Product
Human Otc Drug

Acetaminophen Diphenhydramine Hcl
NDC 0363-9799

Generic Name
Acetaminophen Diphenhydramine Hcl
Dosage Form
Tablet
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

WALGREEN COMPANY

NDC Product
Human Otc Drug

Gentle Laxative
NDC 0363-1634

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

Milk Of Magnesia Cherry
NDC 0363-1648

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

WALGREENS CO.

NDC Product
Human Otc Drug

Walgreen Ultra Strength Pink Bismuth
NDC 0363-7070

Generic Name
Bismuth Subsalicylate
Dosage Form
Suspension
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Acetaminophen Diphenhydramine Hcl
NDC 0363-9664

Generic Name
Acetaminophen Diphenhydramine Hcl
Dosage Form
Tablet
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Walgreen Company

NDC Product
Human Otc Drug

Lansoprazole
NDC 0363-1212

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

Allergy Relief
NDC 0363-1900

Generic Name
Diphenhydramine Hcl
Dosage Form
Capsule
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Diphenhydramine Hydrochloride
NDC 0363-8350

Generic Name
Diphenhydramine Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Diphenhydramine Hydrochloride
NDC 0363-9835

Generic Name
Diphenhydramine Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Walgreens

NDC Product
Human Otc Drug

Soothe
NDC 0363-0073

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

Soothe
NDC 0363-0736

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

Stomach Relief
NDC 0363-7024

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

Soothe Ultra Strength
NDC 0363-7370

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

Walgreens company

NDC Product
Human Otc Drug

Lansoprazole
NDC 0363-0037

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

External Clinical & Regulatory Resources

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