GLYCERYL MONO- AND DICAPRYLOCAPRATE
UNII U72Q2I8C85

Substance Identification & Data

This profile provides standardized clinical and technical data for Glyceryl Mono- And Dicaprylocaprate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) U72Q2I8C85.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 85536-07-8 and the RxNorm Concept ID (RxCUI) 1307310. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
U72Q2I8C85
CAS Registry Number
85536-07-8
RxNorm Concept ID
1307310

Detailed Substance Profile

Preferred Name
GLYCERYL MONO- AND DICAPRYLOCAPRATE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
U72Q2I8C85
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
C83584
National Cancer Institute reference terminology for clinical and research data.
Substance Type
mixture
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Glyceryl Mono- And Dicaprylocaprate. 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

CAPRYLIC(CAPRIC MONO)DIGLCYERIDES
CAPRYLIC/CAPRIC MONO/DIGLYCERIDES
CAPRYLIC/CAPRIC MONO/DI-GLYCERIDES
CAPRYLIC/CAPRIC MONO/DIGLYCERIDES [II]
CAPRYLIC/CAPRIC MONO/DI-GLYCERIDES [II]
GLYCERIDES, C8-10 MONO- AND DI-
GLYCERIDES, C8-10 MONOGLYCERIDES AND DIGLYCERIDES
GLYCERYL CAPRYLOCAPRATE
GLYCERYL MONO AND DICAPRYLOCAPRATE
GLYCERYL MONO- AND DICAPRYLOCAPRATE
GLYCERYL MONO AND DICAPRYLOCAPRATE [USP-RS]
GLYCERYL MONOCAPRYLOCAPRATE TYPE I
MEDIUM CHAIN MONO AND DIGLYCERIDES
MONO AND DIGLYCERIDES OF CAPRYLIC/CAPRIC ACIDS
MONO/DIGLYCERIDES OF CAPRYLIC/CAPRIC ACID

Brand / Trade Names

AKOLINE HH
CAPMUL MCM
IMWITOR 742
MCE 8060
WITAFROL 7420

Systematic Nomenclature

DIGLYCERIDES, C8-10 MONOGLYCERIDES AND DIGLYCERIDES

NDC Products Containing GLYCERYL MONO- AND DICAPRYLOCAPRATE

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 (244), only Active Listings are currently displayed.
→ A-S Medication Solutions 7
→ Acella Pharmaceuticals, LLC 1
→ Advanced Derm Solutions LLC 1
→ Allergan, Inc. 1
→ Almirall, LLC 2
→ Ascend Laboratories, LLC 2
→ Asclemed USA, Inc. 2
→ Aurobindo Pharma Limited 10
→ Aurohealth LLC 4
→ Banner Life Sciences LLC 1
→ Banyan Pharma LLC 1
→ Biocon Pharma Inc. 6
→ Bionpharma Inc. 1
→ BluePoint Laboratories 6
→ BridgeBio Pharma, Inc. 1
→ Bryant Ranch Prepack 10
→ CVS HEALTH CORP 1
→ CVS Pharmacy 1
→ Camber Pharmaceuticals, Inc. 1
→ Cosette Pharmaceuticals, Inc. 2
→ Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) 1
→ EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC) 1
→ Ecolab Inc. 3
→ Encube Ethicals, Inc. 1
→ Epic Pharma, LLC 1
→ Florida Pharmaceutical Products, LLC 1
→ Guardian Drug Company 1
→ Helsinn Therapeutics (U.S.), Inc. 1
→ Indoco Remedies Limited 1
→ KROGER COMPANY 1
→ KalVista Pharmaceuticals Ltd 1
→ Kinfield, Inc. 3
→ Mayne Pharma 1
→ Mayne Pharma LLC 1
→ Micro Labs Limited 1
→ Novugen Pharma (USA) LLC 3
→ NuCare Pharmaceuticals, Inc. 3
→ NuCare Pharmaceuticals,Inc. 1
→ PML NYC, LLC 28
→ Performance Food Group 1
→ Prasco Laboratories 1
→ Proficient Rx LP 2
→ SMART SENSE (KMART) 1
→ Slate Run Pharmaceuticals, LLC 10
→ Sun Pharmaceutical Industries, Inc. 5
→ Supergoop LLC 1
→ TARGET CORPORATION 1
→ TARGET Corporation 1
→ TIME CAP LABORATORIES INC 1
→ Teva Pharmaceuticals USA, Inc. 1
→ The Center Brands, LLC 2
→ The Hain Celestial Group, Inc. 1
→ Viona Pharmaceuticals Inc 1
→ WALGREEN CO. 1
→ WALGREENS 1
→ Waylis Therapeutics LLC 1
→ XLCare Pharmaceuticals, Inc. 1
→ Zydus Lifesciences Limited 20
→ Zydus Pharmaceuticals USA Inc. 16

A-S Medication Solutions

NDC Product
Human Prescription Drug

Estrace
NDC 50090-2321

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Estradiol
NDC 50090-3327

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dutasteride
NDC 50090-4010

Generic Name
Dutasteride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Leflunomide
NDC 50090-5992

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

Estradiol Vaginal
NDC 50090-6811

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dutasteride
NDC 50090-7305

Generic Name
Dutasteride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dutasteride
NDC 50090-7852

Generic Name
Dutasteride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing

Acella Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Sodium Sulfacetamide
NDC 42192-129

Generic Name
Sodium Sulfacetamide
Dosage Form
Liquid
Route
Topical
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Advanced Derm Solutions LLC

NDC Product
Human Otc Drug

Dermeleve
NDC 81507-002

Generic Name
Aluminum Acetate
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Allergan, Inc.

NDC Product
Human Prescription Drug

Estrace
NDC 0430-3754

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
Marketing
ANDA
Active Listing

Almirall, LLC

NDC Product
Human Prescription Drug

Tazorac
NDC 16110-915

Generic Name
Tazarotene
Dosage Form
Cream
Route
Cutaneous
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Tazorac
NDC 16110-916

Generic Name
Tazarotene
Dosage Form
Cream
Route
Cutaneous
Marketing
NDA
Active Listing

Ascend Laboratories, LLC

NDC Product
Human Prescription Drug

Esomeprazole Magnesium
NDC 67877-571

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

Esomeprazole Magnesium
NDC 67877-572

Generic Name
Esomeprazole Magnesium Delayed Release Capsules
Dosage Form
Capsule, Coated Pellets
Route
Oral
Marketing
ANDA
Active Listing

Asclemed USA, Inc.

NDC Product
Human Prescription Drug

Esomeprazole Magnesium
NDC 76420-226

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

Esomeprazole Magnesium
NDC 76420-227

Generic Name
Esomeprazole Magnesium Delayed Release Capsules
Dosage Form
Capsule, Coated Pellets
Route
Oral
Marketing
ANDA
Active Listing

Aurobindo Pharma Limited

NDC Product
Human Prescription Drug

Dutasteride
NDC 59651-021

Generic Name
Dutasteride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dapagliflozin And Metformin Hydrochloride
NDC 59651-154

Generic Name
Dapagliflozin And Metformin Hydrochloride
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dapagliflozin And Metformin Hydrochloride
NDC 59651-155

Generic Name
Dapagliflozin And Metformin Hydrochloride
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dapagliflozin And Metformin Hydrochloride
NDC 59651-156

Generic Name
Dapagliflozin And Metformin Hydrochloride
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dapagliflozin And Metformin Hydrochloride
NDC 59651-157

Generic Name
Dapagliflozin And Metformin Hydrochloride
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dapagliflozin
NDC 59651-159

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

Dapagliflozin
NDC 59651-160

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

Leflunomide
NDC 59651-348

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

Leflunomide
NDC 59651-349

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

Aurohealth LLC

NDC Product
Human Otc Drug

Loratadine
NDC 58602-818

Generic Name
Loratadine
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Pseudoephedrine Hydrochloride
NDC 58602-884

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

Banner Life Sciences LLC

NDC Product
Human Prescription Drug

Bafiertam
NDC 69387-001

Generic Name
Monomethyl Fumarate
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing

Banyan Pharma LLC

NDC Product
Human Prescription Drug

Dutasteride
NDC 84091-100

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

Biocon Pharma Inc.

NDC Product
Human Prescription Drug

Dasatinib
NDC 70377-083

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

Dasatinib
NDC 70377-084

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

Dasatinib
NDC 70377-085

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

Dasatinib
NDC 70377-086

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

Dasatinib
NDC 70377-087

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

Dasatinib
NDC 70377-088

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

Bionpharma Inc.

NDC Product
Human Otc Drug

Loratadine
NDC 69452-283

Generic Name
Loratadine
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing

BluePoint Laboratories

NDC Product
Human Prescription Drug

Dasatinib
NDC 68001-660

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

Dasatinib
NDC 68001-661

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

Dasatinib
NDC 68001-662

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

Dasatinib
NDC 68001-663

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

Dasatinib
NDC 68001-664

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

Dasatinib
NDC 68001-665

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

BridgeBio Pharma, Inc.

NDC Product
Human Prescription Drug

Attruby
NDC 82228-712

Generic Name
Acoramidis Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing

Bryant Ranch Prepack

NDC Product
Human Prescription Drug

Dutasteride
NDC 63629-1222

Generic Name
Dutasteride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dutasteride
NDC 63629-1223

Generic Name
Dutasteride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Aspirin And Extended-release Dipyridamole
NDC 63629-5045

Generic Name
Aspirin And Extended-release Dipyridamole
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dutasteride
NDC 63629-8207

Generic Name
Dutasteride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Leflunomide
NDC 63629-9728

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

Esomeprazole Magnesium
NDC 71335-1335

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

Esomeprazole Magnesium
NDC 71335-1368

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

Leflunomide
NDC 71335-2256

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

Esomeprazole Magnesium
NDC 71335-9678

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

Dutasteride
NDC 72162-1296

Generic Name
Dutasteride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing

CVS HEALTH CORP

NDC Product
Human Otc Drug

Loratadine
NDC 69842-686

Generic Name
Loratadine
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing

CVS Pharmacy

NDC Product
Human Otc Drug

Headache Relief Extra Strength
NDC 69842-586

Generic Name
Acetaminophen, Aspirin, Caffeine
Dosage Form
Tablet
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Camber Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Dutasteride
NDC 31722-131

Generic Name
Dutasteride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing

Cosette Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Welchol
NDC 0713-0880

Generic Name
Colesevelam Hydrochloride
Dosage Form
For Suspension
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Colesevelam Hydrochloride
NDC 0713-0935

Generic Name
Colesevelam Hydrochloride
Dosage Form
For Suspension
Route
Oral
Marketing
NDA
Active Listing

Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)

NDC Product
Human Otc Drug

Headache Relief Extra Strength
NDC 55910-686

Generic Name
Acetaminophen, Aspirin, Caffeine
Dosage Form
Tablet
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

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

NDC Product
Human Otc Drug

Headache Relief Extra Strength
NDC 49035-786

Generic Name
Acetaminophen, Aspirin, Caffeine
Dosage Form
Tablet
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Ecolab Inc.

NDC Product
Human Otc Drug

Swisher
NDC 47593-591

Generic Name
Benzalkonium Chloride
Dosage Form
Solution
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Ssdc Antibacterial Foam Handsoap
NDC 47593-663

Generic Name
Benzalkonium Chloride
Dosage Form
Solution
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Encube Ethicals, Inc.

NDC Product
Human Prescription Drug

Estradiol Vaginal
NDC 21922-085

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
Marketing
ANDA
Active Listing

Epic Pharma, LLC

NDC Product
Human Prescription Drug

Dutasteride
NDC 42806-549

Generic Name
Dutasteride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing

Florida Pharmaceutical Products, LLC

NDC Product
Human Prescription Drug

Lofexidine
NDC 71921-250

Generic Name
Lofexidine
Dosage Form
Tablet, Coated
Route
Oral
Marketing
ANDA
Active Listing

Guardian Drug Company

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 53041-666

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

Helsinn Therapeutics (U.S.), Inc.

NDC Product
Human Prescription Drug

Akynzeo
NDC 69639-101

Generic Name
Netupitant And Palonosetron
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing

Indoco Remedies Limited

NDC Product
Human Prescription Drug

Lofexidine
NDC 14445-146

Generic Name
Lofexidine
Dosage Form
Tablet, Coated
Route
Oral
Marketing
ANDA
Active Listing

KROGER COMPANY

NDC Product
Human Otc Drug

Loratadine
NDC 41226-686

Generic Name
Loratadine
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing

KalVista Pharmaceuticals Ltd

NDC Product
Human Prescription Drug

Ekterly
NDC 82928-300

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

Kinfield, Inc.

NDC Product
Human Otc Drug

Kinfield Relief Balm Anti-itch Remedy
NDC 81750-020

Generic Name
Kinfield Relief Balm Anti-itch Remedy
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Mayne Pharma

NDC Product
Human Prescription Drug

Bijuva
NDC 68308-751

Generic Name
Estradiol And Progesterone
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing

Mayne Pharma LLC

NDC Product
Human Prescription Drug

Bijuva
NDC 50261-211

Generic Name
Estradiol And Progesterone
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing

Micro Labs Limited

NDC Product
Human Prescription Drug

Aspirin And Extended-release Dipyridamole
NDC 42571-274

Generic Name
Aspirin And Extended-release Dipyridamole
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Novugen Pharma (USA) LLC

NDC Product
Human Prescription Drug

Sacubitril And Valsartan
NDC 82293-027

Generic Name
Sacubitril And Valsartan
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Sacubitril And Valsartan
NDC 82293-028

Generic Name
Sacubitril And Valsartan
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Sacubitril And Valsartan
NDC 82293-029

Generic Name
Sacubitril And Valsartan
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

NuCare Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Dutasteride
NDC 68071-3732

Generic Name
Dutasteride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dutasteride
NDC 68071-3757

Generic Name
Dutasteride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dutasteride
NDC 68071-3857

Generic Name
Dutasteride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing

NuCare Pharmaceuticals,Inc.

NDC Product
Human Prescription Drug

Dutasteride
NDC 68071-4821

Generic Name
Dutasteride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing

PML NYC, LLC

Performance Food Group

Prasco Laboratories

NDC Product
Human Prescription Drug

Estradiol Vaginal Cream
NDC 66993-002

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
Marketing
ANDA
Active Listing

Proficient Rx LP

NDC Product
Human Prescription Drug

Dutasteride
NDC 71205-278

Generic Name
Dutasteride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Esomeprazole Magnesium
NDC 71205-706

Generic Name
Esomeprazole Magnesium Delayed Release Capsules
Dosage Form
Capsule, Coated Pellets
Route
Oral
Marketing
ANDA
Active Listing

SMART SENSE (KMART)

NDC Product
Human Otc Drug

Loratadine
NDC 49738-686

Generic Name
Loratadine
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing

Slate Run Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Potassium Chloride
NDC 70436-152

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

Potassium Chloride
NDC 70436-153

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

Mycophenolic Acid
NDC 70436-172

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

Mycophenolic Acid
NDC 70436-173

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

Diltiazem Hydrochloride
NDC 70436-195

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

Diltiazem Hydrochloride
NDC 70436-196

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

Diltiazem Hydrochloride
NDC 70436-197

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

Diltiazem Hydrochloride
NDC 70436-198

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

Diltiazem Hydrochloride
NDC 70436-199

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

Diltiazem Hydrochloride
NDC 70436-200

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

Sun Pharmaceutical Industries, Inc.

NDC Product
Human Prescription Drug

Winlevi
NDC 47335-994

Generic Name
Clascoterone
Dosage Form
Cream
Route
Topical
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Fluphenazine Hydrochloride
NDC 51672-4233

Generic Name
Fluphenazine Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fluphenazine Hydrochloride
NDC 51672-4234

Generic Name
Fluphenazine Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fluphenazine Hydrochloride
NDC 51672-4235

Generic Name
Fluphenazine Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fluphenazine Hydrochloride
NDC 51672-4236

Generic Name
Fluphenazine Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Supergoop LLC

TARGET CORPORATION

NDC Product
Human Otc Drug

Allergy Relief
NDC 11673-986

Generic Name
Loratadine
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing

TARGET Corporation

NDC Product
Human Otc Drug

Headache Relief Extra Strength
NDC 11673-686

Generic Name
Acetaminophen, Aspirin, Caffeine
Dosage Form
Tablet
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

TIME CAP LABORATORIES INC

NDC Product
Human Otc Drug

Loratadine
NDC 49483-686

Generic Name
Loratadine
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Estradiol
NDC 0093-3541

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
Marketing
ANDA
Active Listing

The Center Brands, LLC

The Hain Celestial Group, Inc.

Viona Pharmaceuticals Inc

NDC Product
Human Prescription Drug

Ibuprofen And Famotidine
NDC 72578-214

Generic Name
Ibuprofen And Famotidine
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

WALGREEN CO.

NDC Product
Human Otc Drug

Pseudoephedrine Hydrochloride
NDC 0363-6611

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

WALGREENS

NDC Product
Human Otc Drug

Wal-itin
NDC 0363-1686

Generic Name
Loratadine
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing

Waylis Therapeutics LLC

NDC Product
Human Prescription Drug

Avodart
NDC 80725-712

Generic Name
Dutasteride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
NDA
Active Listing

XLCare Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Dutasteride
NDC 72865-140

Generic Name
Dutasteride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing

Zydus Lifesciences Limited

NDC Product
Human Prescription Drug

Esomeprazole Magnesium
NDC 70771-1493

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

Esomeprazole Magnesium
NDC 70771-1494

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

Dimethyl Fumarate
NDC 70771-1530

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

Dimethyl Fumarate
NDC 70771-1531

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

Brivaracetam
NDC 70771-1754

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

Brivaracetam
NDC 70771-1755

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

Brivaracetam
NDC 70771-1756

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

Brivaracetam
NDC 70771-1757

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

Brivaracetam
NDC 70771-1758

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

Dasatinib
NDC 70771-1901

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

Dasatinib
NDC 70771-1902

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

Dasatinib
NDC 70771-1903

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

Dasatinib
NDC 70771-1904

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

Dasatinib
NDC 70771-1905

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

Dasatinib
NDC 70771-1906

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

Ibuprofen And Famotidine
NDC 70771-1924

Generic Name
Ibuprofen And Famotidine
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Zydus Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Esomeprazole Magnesium
NDC 68382-441

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

Esomeprazole Magnesium
NDC 68382-442

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

Dimethyl Fumarate
NDC 70710-1204

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

Dimethyl Fumarate
NDC 70710-1205

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

Brivaracetam
NDC 70710-1584

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

Brivaracetam
NDC 70710-1585

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

Brivaracetam
NDC 70710-1586

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

Brivaracetam
NDC 70710-1587

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

Brivaracetam
NDC 70710-1588

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

Dasatinib
NDC 70710-1741

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

Dasatinib
NDC 70710-1742

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

Dasatinib
NDC 70710-1743

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

Dasatinib
NDC 70710-1744

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

Dasatinib
NDC 70710-1745

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

Dasatinib
NDC 70710-1746

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

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