HYPROMELLOSE 2910 (5 MPA.S)
UNII R75537T0T4

Substance Identification & Data

This profile provides standardized clinical and technical data for Hypromellose 2910 (5 Mpa.s), uniquely identified by the FDA Unique Ingredient Identifier (UNII) R75537T0T4.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9004-65-3 and the RxNorm Concept ID (RxCUI) 1300452. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
R75537T0T4
CAS Registry Number
9004-65-3
RxNorm Concept ID
1300452

Detailed Substance Profile

Preferred Name
HYPROMELLOSE 2910 (5 MPA.S)
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
R75537T0T4
The specific atomic composition represented as a molecular structure string.
Substance Type
polymer
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Hypromellose 2910 (5 Mpa.s). 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

HYDROXYPROPYL METHYLCELLULOSE E5
HYDROXYPROPYL METHYLCELLULOSE E5 [II]
HYPROMELLOSE 2910 (4.5 MPA.S)
HYPROMELLOSE 2910 (5 CPS)
HYPROMELLOSE 2910 (5 MPA.S)
HYPROMELLOSE 2910 (5 MPA.S) [II]
HYPROMELLOSE E5
METHOCEL E5 PREMIUM

Brand / Trade Names

BENECEL HPMC E5
DOW METHOCEL E5
METHOCEL E5
PHARMACOAT 645

NDC Products Containing HYPROMELLOSE 2910 (5 MPA.S)

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.
→ 7-Eleven 1
→ Accord Healthcare, Inc. 1
→ Actavis Pharma, Inc. 10
→ AiPing Pharmaceutical, Inc. 1
→ Amneal Pharmaceuticals of New York LLC 6
→ AstraZeneca Pharmaceuticals LP 3
→ Contract Pharmacal Corp. 2
→ Endo USA, Inc. 7
→ Hikma Pharmaceuticals USA Inc. 8
→ Indoco Remedies Limited 3
→ Lannett Company, Inc. 10
→ MAJOR PHARMACEUTICALS 5
→ Major Pharmaceuticals 25
→ Marlex Pharmaceuticals Inc 1
→ Merck Sharp & Dohme LLC 3
→ Mylan Pharmaceuticals Inc. 1
→ NCS HealthCare of KY, LLC dba Vangard Labs 14
→ NorthStar Rx LLC 11
→ NorthStar RxLLC 1
→ Northstar Rx LLC 8
→ Northstar Rx LLC. 1
→ Rising Pharma Holdings, Inc. 4
→ Rugby Laboratories 1
→ Sandoz Inc 6
→ Sun Pharmaceutical Industries, Inc. 4
→ TARGET CORPORATION 2
→ Teva Pharmaceuticals USA, Inc. 23
→ Teva Pharmaceuticals, Inc. 16
→ Torrent Pharmaceuticals Limited 8
→ Trigen Laboratories, LLC 4
→ WALGREEN CO. 6
→ WALGREEN COMPANY 1
→ Walgreens 2
→ Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. 1

7-Eleven

NDC Product
Human Otc Drug

Acid Reducer
NDC 10202-722

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

Accord Healthcare, Inc.

NDC Product
Human Prescription Drug

Simvastatin
NDC 16729-004

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

Actavis Pharma, Inc.

NDC Product
Drug For Further Processing

NDC 0591-4101

Generic Name
Perphenazine
Dosage Form
Tablet, Film Coated
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Perphenazine
NDC 0591-4101

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

Perphenazine
NDC 0591-4102

Generic Name
Perphenazine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0591-4102

Generic Name
Perphenazine
Dosage Form
Tablet, Film Coated
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing

NDC 0591-4103

Generic Name
Perphenazine
Dosage Form
Tablet, Film Coated
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Perphenazine
NDC 0591-4103

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

Perphenazine
NDC 0591-4104

Generic Name
Perphenazine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0591-4104

Generic Name
Perphenazine
Dosage Form
Tablet, Film Coated
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Doxycycline Hyclate
NDC 0591-4550

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

Doxycycline Hyclate
NDC 0591-4575

Generic Name
Doxycycline Hyclate
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

AiPing Pharmaceutical, Inc.

NDC Product
Human Prescription Drug

Doxycycline
NDC 11788-134

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

Amneal Pharmaceuticals of New York LLC

AstraZeneca Pharmaceuticals LP

NDC Product
Human Prescription Drug

Xigduo Xr
NDC 0310-6225

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

Xigduo Xr
NDC 0310-6250

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

Xigduo Xr
NDC 0310-6260

Generic Name
Dapagliflozin And Metformin Hydrochloride
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
NDA
Active Listing

Contract Pharmacal Corp.

NDC Product
Human Prescription Drug

Famotidine
NDC 10267-5689

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

Famotidine
NDC 10267-5690

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

Endo USA, Inc.

NDC Product
Human Prescription Drug

Nitisinone
NDC 0254-3020

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

Nitisinone
NDC 0254-3021

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

Nitisinone
NDC 0254-3022

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

Topiramate
NDC 10370-365

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

Topiramate
NDC 10370-366

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

Topiramate
NDC 10370-367

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

Topiramate
NDC 10370-368

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

Hikma Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Everolimus
NDC 0054-0470

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

Everolimus
NDC 0054-0471

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

Everolimus
NDC 0054-0472

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

Everolimus
NDC 0054-0480

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

Everolimus
NDC 0054-0481

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

Everolimus
NDC 0054-0497

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

Amoxicillin And Clavulanate Potassium
NDC 0143-9981

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

Amoxicillin And Clavulanate Potassium
NDC 0143-9982

Generic Name
Amoxicillin And Clavulanate Potassium
Dosage Form
Powder, For Suspension
Route
Oral
Marketing
ANDA
Active Listing

Indoco Remedies Limited

NDC Product
Human Prescription Drug

Varenicline Tartrate
NDC 14445-153

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

Varenicline Tartrate
NDC 14445-154

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

Varenicline
NDC 14445-155

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

Lannett Company, Inc.

NDC Product
Human Prescription Drug

Propranolol Hydrochloride
NDC 0527-4116

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

Propranolol Hydrochloride
NDC 0527-4117

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

Propranolol Hydrochloride
NDC 0527-4118

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

Propranolol Hydrochloride
NDC 0527-4119

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

MAJOR PHARMACEUTICALS

NDC Product
Human Prescription Drug

Lurasidone Hydrochloride
NDC 0904-7421

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

Lurasidone Hydrochloride
NDC 0904-7422

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

Lurasidone Hydrochloride
NDC 0904-7423

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

Lurasidone Hydrochloride
NDC 0904-7424

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

Lurasidone Hydrochloride
NDC 0904-7425

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

Major Pharmaceuticals

NDC Product
Human Prescription Drug

Ondansetron
NDC 0904-6551

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

Ondansetron
NDC 0904-6552

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

Imatinib Mesylate
NDC 0904-6621

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

Quetiapine
NDC 0904-6639

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

Quetiapine
NDC 0904-6640

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

Quetiapine
NDC 0904-6641

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

Quetiapine
NDC 0904-6642

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

Quetiapine
NDC 0904-6643

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

Imatinib Mesylate
NDC 0904-6901

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

Tacrolimus
NDC 0904-7097

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

Rivastigmine Tartrate
NDC 0904-7107

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

Sirolimus
NDC 0904-7248

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

Lurasidone Hydrochloride
NDC 0904-7355

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

Lurasidone Hydrochloride
NDC 0904-7356

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

Lurasidone Hydrochloride
NDC 0904-7357

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

Lurasidone Hydrochloride
NDC 0904-7358

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

Lurasidone Hydrochloride
NDC 0904-7359

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

Prochlorperazine Maleate
NDC 0904-7381

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

Prochlorperazine Maleate
NDC 0904-7382

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

Varenicline
NDC 0904-7413

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

Varenicline
NDC 0904-7414

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

Varenicline
NDC 0904-7415

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

Venlafaxine Hydrochloride
NDC 0904-7487

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

Venlafaxine Hydrochloride
NDC 0904-7488

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

Venlafaxine Hydrochloride
NDC 0904-7489

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

Marlex Pharmaceuticals Inc

NDC Product
Human Prescription Drug

Levocetirizine Dihydrochloride
NDC 10135-639

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

Merck Sharp & Dohme LLC

NDC Product
Human Prescription Drug

Verquvo
NDC 0006-5028

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

Verquvo
NDC 0006-5029

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

Verquvo
NDC 0006-5030

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

Mylan Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Sorafenib Tosylate
NDC 0378-1201

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

NCS HealthCare of KY, LLC dba Vangard Labs

NDC Product
Human Prescription Drug

Ondansetron Hydrochloride
NDC 0615-8185

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

Carvedilol
NDC 0615-8387

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

Carvedilol
NDC 0615-8388

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

Carvedilol
NDC 0615-8389

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

Carvedilol
NDC 0615-8390

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

Escitalopram
NDC 0615-8475

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

Escitalopram
NDC 0615-8476

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

Escitalopram
NDC 0615-8477

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

Venlafaxine Hydrochloride
NDC 0615-8509

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

Venlafaxine Hydrochloride
NDC 0615-8510

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

Bupropion Hydrochloride
NDC 0615-8601

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

Bupropion Hydrochloride
NDC 0615-8602

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

Ranolazine
NDC 0615-8611

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

Ciprofloxacin
NDC 0615-8630

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

NorthStar Rx LLC

NDC Product
Human Prescription Drug

Paroxetine
NDC 16714-183

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

Paroxetine
NDC 16714-184

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

Raloxifene Hydrochloride
NDC 16714-213

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

Amoxicillin And Clavulanate Potassium
NDC 16714-295

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

Amoxicillin And Clavulanate Potassium
NDC 16714-296

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

Amoxicillin And Clavulanate Potassium
NDC 16714-297

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

Cefprozil
NDC 16714-399

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

Zolpidem Tartrate
NDC 16714-621

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

Zolpidem Tartrate
NDC 16714-622

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

Terbinafine
NDC 16714-795

Generic Name
Terbinafine Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

NorthStar RxLLC

NDC Product
Human Prescription Drug

Itraconazole
NDC 16714-743

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

Northstar Rx LLC

NDC Product
Human Prescription Drug

Chlorpromazine Hydrochloride
NDC 16714-047

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

Chlorpromazine Hydrochloride
NDC 16714-048

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

Chlorpromazine Hydrochloride
NDC 16714-049

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

Chlorpromazine Hydrochloride
NDC 16714-050

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

Chlorpromazine Hydrochloride
NDC 16714-051

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

Diltiazem Hydrochloride
NDC 16714-553

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

Diltiazem Hydrochloride
NDC 16714-554

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

Diltiazem Hydrochloride
NDC 16714-555

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

Northstar Rx LLC.

NDC Product
Human Prescription Drug

Colchicine
NDC 16714-039

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

Rising Pharma Holdings, Inc.

NDC Product
Human Prescription Drug

Itraconazole
NDC 16571-245

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

Darifenacin
NDC 16571-767

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

Darifenacin
NDC 16571-768

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

Esomeprazole Magnesium
NDC 16571-880

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

Rugby Laboratories

NDC Product
Human Otc Drug

Acid Reducer
NDC 0536-1322

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

Sandoz Inc

NDC Product
Human Prescription Drug

Amoxicillin
NDC 0781-5061

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

Mycophenolate Mofetil
NDC 0781-5175

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

Amoxicillin
NDC 0781-6039

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

Amoxicillin
NDC 0781-6041

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

Amoxicillin
NDC 0781-6156

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

Amoxicillin
NDC 0781-6157

Generic Name
Amoxicillin
Dosage Form
Powder, For Suspension
Route
Oral
Marketing
ANDA
Active Listing

Sun Pharmaceutical Industries, Inc.

NDC Product
Human Prescription Drug

Kapspargo
NDC 10631-008

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

Kapspargo
NDC 10631-009

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

Kapspargo
NDC 10631-010

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

Kapspargo
NDC 10631-011

Generic Name
Metoprolol Succinate
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA
Active Listing

TARGET CORPORATION

NDC Product
Human Otc Drug

Guaifenesin
NDC 11673-539

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

Guaifenesin
NDC 11673-840

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

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Carvedilol
NDC 0093-0051

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

Carvedilol
NDC 0093-0135

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

Etodolac
NDC 0093-1118

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

Etodolac
NDC 0093-1122

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

Amoxicillin And Clavulanate Potassium
NDC 0093-2277

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

Amoxicillin And Clavulanate Potassium
NDC 0093-2279

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

Risedronate Sodium
NDC 0093-3098

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

Risedronate Sodium
NDC 0093-3099

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

Risedronate Sodium
NDC 0093-3100

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

Erythromycin
NDC 0093-5571

Generic Name
Erythromycin
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0093-5571

Generic Name
Erythromycin
Dosage Form
Tablet, Film Coated
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing

NDC 0093-5572

Generic Name
Erythromycin
Dosage Form
Tablet, Film Coated
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Erythromycin
NDC 0093-5572

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

Etodolac
NDC 0093-7172

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

Carvedilol
NDC 0093-7295

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

Carvedilol
NDC 0093-7296

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

Anastrozole
NDC 0093-7536

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

Levocetirizine Dihydrochloride
NDC 0093-7701

Generic Name
Levocetirizine Dihydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0093-7909

Generic Name
Tiopronin
Dosage Form
Tablet, Sugar Coated
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Tiopronin
NDC 0093-7909

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

Irbesartan And Hydrochlorothiazide
NDC 0093-8232

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

Irbesartan And Hydrochlorothiazide
NDC 0093-8238

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

Amoxicillin And Clavulanate Potassium
NDC 0093-8675

Generic Name
Amoxicillin And Clavulanate Potassium
Dosage Form
Powder, For Suspension
Route
Oral
Marketing
ANDA
Active Listing

Teva Pharmaceuticals, Inc.

NDC Product
Drug For Further Processing

NDC 0480-2299

Generic Name
Phentermine And Topiramate
Dosage Form
Capsule, Extended Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Phentermine And Topiramate
NDC 0480-2299

Generic Name
Phentermine And Topiramate
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Topiramate
NDC 0480-2359

Generic Name
Topiramate
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0480-2359

Generic Name
Topiramate
Dosage Form
Capsule, Extended Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Alvaiz
NDC 0480-3276

Generic Name
Eltrombopag
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0480-3295

Generic Name
Phentermine And Topiramate
Dosage Form
Capsule, Extended Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Phentermine And Topiramate
NDC 0480-3295

Generic Name
Phentermine And Topiramate
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Phentermine And Topiramate
NDC 0480-3296

Generic Name
Phentermine And Topiramate
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0480-3296

Generic Name
Phentermine And Topiramate
Dosage Form
Capsule, Extended Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing

NDC 0480-3297

Generic Name
Phentermine And Topiramate
Dosage Form
Capsule, Extended Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Phentermine And Topiramate
NDC 0480-3297

Generic Name
Phentermine And Topiramate
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Sorafenib
NDC 0480-5425

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

Torrent Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Tolterodine Tartrate
NDC 13668-189

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

Tolterodine Tartrate
NDC 13668-190

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

Itraconazole
NDC 13668-463

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

Lurasidone Hydrochloride
NDC 13668-509

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

Aprepitant
NDC 13668-591

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

Aprepitant
NDC 13668-592

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

Aprepitant
NDC 13668-593

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

Aprepitant
NDC 13668-594

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

Trigen Laboratories, LLC

NDC Product
Human Prescription Drug

Hydromorphone Hydrochloride
NDC 13811-701

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

Hydromorphone Hydrochloride
NDC 13811-702

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

Hydromorphone Hydrochloride
NDC 13811-703

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

Hydromorphone Hydrochloride
NDC 13811-704

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

WALGREEN CO.

NDC Product
Human Otc Drug

Acid Reducer
NDC 0363-1008

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

Famotidine
NDC 0363-1899

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

Famotidine
NDC 0363-4400

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

Famotidine
NDC 0363-5300

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

Famotidine
NDC 0363-9607

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

WALGREEN COMPANY

NDC Product
Human Otc Drug

Hives Relief
NDC 0363-6340

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

Walgreens

NDC Product
Human Otc Drug

Guaifenesin
NDC 0363-0570

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

Guaifenesin
NDC 0363-9569

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

Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.

NDC Product
Human Prescription Drug

Protonix Delayed-release
NDC 0008-0844

Generic Name
Pantoprazole Sodium
Dosage Form
Granule, Delayed Release
Route
Oral
Marketing
NDA
Active Listing

External Clinical & Regulatory Resources

CAS
Common Chemistry
NCATS
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NCATS
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