HYPROMELLOSE 2910 (6 MPA.S)
UNII 0WZ8WG20P6

Substance Identification & Data

This profile provides standardized clinical and technical data for Hypromellose 2910 (6 Mpa.s), uniquely identified by the FDA Unique Ingredient Identifier (UNII) 0WZ8WG20P6.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9004-65-3 and the RxNorm Concept ID (RxCUI) 1300454. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
0WZ8WG20P6
CAS Registry Number
9004-65-3
RxNorm Concept ID
1300454

Detailed Substance Profile

Preferred Name
HYPROMELLOSE 2910 (6 MPA.S)
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
0WZ8WG20P6
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 (6 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

BENECEL HPMC E6
HYDROXYPROPYL METHYLCELLULOSE 2910 (6 CPS)
HYDROXYPROPYL METHYLCELLULOSE 606
HYDROXYPROPYL METHYLCELLULOSE 606 [II]
HYDROXYPROPYL METHYLCELLULOSE 6CP
HYPROMELLOSE 2910 (6 CPS)
HYPROMELLOSE 2910 (6 MPA.S)
HYPROMELLOSE 2910 (6 MPA.S) [II]
HYPROMELLOSE 606
HYPROMELLOSE 6CP
HYPROMELLOSE E6
PHARMACOAT 606 [II]

Brand / Trade Names

METHOCEL E6
PHARMACOAT 606
PHARMACOAT 606G

NDC Products Containing HYPROMELLOSE 2910 (6 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.
→ Actavis Pharma, Inc. 22
→ Amneal Pharmaceuticals of New York LLC 15
→ Astellas Pharma US, Inc. 6
→ Endo USA, Inc. 1
→ Hikma Pharmaceuticals USA Inc 2
→ Hikma Pharmaceuticals USA Inc. 1
→ Merck Sharp & Dohme LLC 14
→ Mylan Pharmaceuticals Inc. 3
→ NCS HealthCare of KY, Inc dba Vangard Labs 2
→ NCS HealthCare of KY, LLC dba Vangard Labs 5
→ Padagis US LLC 4
→ Pfizer Laboratories Div Pfizer Inc 11
→ RUGBY LABORATORIES 1
→ Rugby Laboratories 1
→ SpecGx LLC 5
→ Teva Pharmaceuticals USA, Inc. 63
→ Teva Pharmaceuticals, Inc. 15
→ Upsher-Smith Laboratories, LLC 5
→ WALGREEN CO 1
→ WALGREEN CO. 4
→ WALGREENS 1
→ WALGREENS CO. 1
→ Walgreens 1
→ Walgreens Company 3
→ Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. 13

Actavis Pharma, Inc.

NDC Product
Human Prescription Drug

Verapamil Hydrochloride
NDC 0591-0343

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

NDC 0591-0343

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

Verapamil Hydrochloride
NDC 0591-0345

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

NDC 0591-0345

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

Verapamil Hydrochloride
NDC 0591-0404

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

NDC 0591-0404

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

Mesalamine
NDC 0591-2245

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

Budesonide
NDC 0591-2510

Generic Name
Budesonide
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
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

Solifenacin Succinate
NDC 0591-3795

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

Solifenacin Succinate
NDC 0591-3796

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

Vigabatrin
NDC 0591-3851

Generic Name
Vigabatrin
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
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
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 0591-4102

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
Human Prescription Drug

Perphenazine
NDC 0591-4103

Generic Name
Perphenazine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
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
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

Perphenazine
NDC 0591-4104

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

Mifepristone
NDC 0591-4390

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

Tranylcypromine Sulfate
NDC 0591-5590

Generic Name
Tranylcypromine Sulfate
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing

Amneal Pharmaceuticals of New York LLC

NDC Product
Human Prescription Drug

Colesevelam Hydrochloride
NDC 0115-1320

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

Cyclobenzaprine Hydrochloride
NDC 0115-1436

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

Cyclobenzaprine Hydrochloride
NDC 0115-1437

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

Terbutaline Sulfate
NDC 0115-2611

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

Terbutaline Sulfate
NDC 0115-2622

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

Colestipol Hydrochloride
NDC 0115-5211

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

Bupropion Hydrochloride
NDC 0115-5445

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

Fenofibrate
NDC 0115-5511

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

Fenofibrate
NDC 0115-5522

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

Astellas Pharma US, Inc.

NDC Product
Human Prescription Drug

Veozah
NDC 0469-2460

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

Myrbetriq
NDC 0469-2601

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

Myrbetriq
NDC 0469-2602

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

Veozah
NDC 0469-2660

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

Veozah
NDC 0469-2760

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

Myrbetriq
NDC 0469-5020

Generic Name
Mirabegron
Dosage Form
Granule, For Suspension, Extended Release
Route
Oral
Marketing
NDA
Active Listing

Endo USA, Inc.

NDC Product
Human Prescription Drug

Penicillamine
NDC 0254-2000

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

Hikma Pharmaceuticals USA Inc

NDC Product
Human Prescription Drug

Prucalopride
NDC 0054-0749

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

Prucalopride
NDC 0054-0750

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

Hikma Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Galantamine Hydrobromide
NDC 0054-0137

Generic Name
Galantamine Hydrobromide
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

Merck Sharp & Dohme LLC

NDC Product
Human Prescription Drug

Janumet Xr
NDC 0006-0078

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

Janumet Xr
NDC 0006-0080

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

Janumet Xr
NDC 0006-0081

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

Isentress
NDC 0006-0473

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

Isentress
NDC 0006-0477

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

Prevymis
NDC 0006-3075

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

Prevymis
NDC 0006-3076

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

Isentress
NDC 0006-3080

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

Isentress
NDC 0006-3603

Generic Name
Raltegravir
Dosage Form
Granule, For Suspension
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Prevymis
NDC 0006-5003

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

Prevymis
NDC 0006-5004

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

Idvynso
NDC 0006-5092

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

Steglatro
NDC 0006-5363

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

Steglatro
NDC 0006-5364

Generic Name
Ertugliflozin
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
NDC Product
Human Prescription Drug

Ferric Citrate
NDC 0378-2895

Generic Name
Ferric Citrate
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Budesonide
NDC 0378-4500

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

NCS HealthCare of KY, Inc dba Vangard Labs

NDC Product
Human Prescription Drug

Mirtazapine
NDC 0615-8268

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

Mirtazapine
NDC 0615-8269

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

NCS HealthCare of KY, LLC dba Vangard Labs

NDC Product
Human Prescription Drug

Isosorbide Mononitrate
NDC 0615-7767

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

Isosorbide Mononitrate
NDC 0615-7768

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

Citalopram
NDC 0615-8022

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

Citalopram
NDC 0615-8023

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

Citalopram
NDC 0615-8141

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

Padagis US LLC

NDC Product
Human Prescription Drug

Hydromorphone Hydrochloride
NDC 0574-0293

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

Hydromorphone Hydrochloride
NDC 0574-0294

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

Hydromorphone Hydrochloride
NDC 0574-0295

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

Hydromorphone Hydrochloride
NDC 0574-0297

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

Pfizer Laboratories Div Pfizer Inc

NDC Product
Human Prescription Drug

Ibrance
NDC 0069-0284

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

Ibrance
NDC 0069-0486

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

Xeljanz Xr
NDC 0069-0501

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

Xeljanz Xr
NDC 0069-0502

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

Ibrance
NDC 0069-0688

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

Xeljanz
NDC 0069-1001

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

Xeljanz
NDC 0069-1002

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

Xeljanz
NDC 0069-1029

Generic Name
Tofacitinib
Dosage Form
Solution
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Paxlovid
NDC 0069-5045

Generic Name
Nirmatrelvir And Ritonavir
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Paxlovid
NDC 0069-5317

Generic Name
Nirmatrelvir And Ritonavir
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Paxlovid
NDC 0069-5321

Generic Name
Nirmatrelvir And Ritonavir
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing

RUGBY LABORATORIES

NDC Product
Human Otc Drug

Acetaminophen And Ibuprofen
NDC 0536-1376

Generic Name
Acetaminophen And Ibuprofen
Dosage Form
Tablet
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

SpecGx LLC

NDC Product
Human Prescription Drug

Prucalopride
NDC 0406-6301

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

Prucalopride
NDC 0406-6302

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

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Cefprozil
NDC 0093-1078

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

Cefaclor
NDC 0093-1087

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

Cyclobenzaprine Hydrochloride
NDC 0093-1920

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

Cyclobenzaprine Hydrochloride
NDC 0093-1921

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

Tri-lo-sprintec
NDC 0093-2140

Generic Name
Norgestimate And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Cephalexin
NDC 0093-2238

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

Cephalexin
NDC 0093-2240

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

Amoxicillin And Clavulanate Potassium
NDC 0093-2274

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 0093-2275

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 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

Lansoprazole
NDC 0093-3008

Generic Name
Lansoprazole
Dosage Form
Tablet, Orally Disintegrating, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Lansoprazole
NDC 0093-3009

Generic Name
Lansoprazole
Dosage Form
Tablet, Orally Disintegrating, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Camrese
NDC 0093-3134

Generic Name
Levonorgestrel / Ethinyl Estradiol And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Reclipsen 28 Day
NDC 0093-3304

Generic Name
Desogestrel And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atorvastatin Calcium
NDC 0093-5056

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

Atorvastatin Calcium
NDC 0093-5057

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

Atorvastatin Calcium
NDC 0093-5058

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

Atorvastatin Calcium
NDC 0093-5059

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

Hydroxyzine Hydrochloride
NDC 0093-5060

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

Hydroxyzine Hydrochloride
NDC 0093-5061

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

Hydroxyzine Hydrochloride
NDC 0093-5062

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

Almotriptan Malate
NDC 0093-5260

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

Almotriptan Malate
NDC 0093-5261

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

Mimvey
NDC 0093-5455

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

Rivelsa
NDC 0093-6031

Generic Name
Levonorgestrel/ethinyl Estradiol And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Camrese Lo
NDC 0093-6148

Generic Name
Levonorgestrel/ethinyl Estradiol And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Drug For Further Processing

NDC 0093-7163

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

Tolterodine Tartrate
NDC 0093-7163

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

Tolterodine Tartrate
NDC 0093-7164

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

NDC 0093-7164

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

Lansoprazole
NDC 0093-7350

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

Lansoprazole
NDC 0093-7351

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

Capecitabine
NDC 0093-7473

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

Capecitabine
NDC 0093-7474

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

Imatinib Mesylate
NDC 0093-7629

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

Imatinib Mesylate
NDC 0093-7630

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

Vardenafil Hydrochloride
NDC 0093-7652

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

Vardenafil Hydrochloride
NDC 0093-7653

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

Vardenafil Hydrochloride
NDC 0093-7654

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

Vardenafil Hydrochloride
NDC 0093-7655

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

Erlotinib
NDC 0093-7663

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

Erlotinib
NDC 0093-7664

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

Famciclovir
NDC 0093-8117

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

NDC 0093-8117

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

Famciclovir
NDC 0093-8118

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

NDC 0093-8118

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

Famciclovir
NDC 0093-8119

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

NDC 0093-8119

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

Quetiapine
NDC 0093-8162

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

Quetiapine
NDC 0093-8163

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

Quetiapine
NDC 0093-8164

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

Quetiapine
NDC 0093-8165

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

Quetiapine
NDC 0093-8166

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

Eletriptan Hydrobromide
NDC 0093-8310

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

Eletriptan Hydrobromide
NDC 0093-8311

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

Diflunisal
NDC 0093-9222

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

Lessina
NDC 0555-9014

Generic Name
Levonorgestrel And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Portia
NDC 0555-9020

Generic Name
Levonorgestrel And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Apri 28 Day
NDC 0555-9043

Generic Name
Desogestrel And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Kariva
NDC 0555-9050

Generic Name
Desogestrel/ethinyl Estradiol And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Velivet Triphasic Regimen
NDC 0555-9051

Generic Name
Desogestrel And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Jolessa
NDC 0555-9123

Generic Name
Levonorgestrel / Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
NDA AUTHORIZED GENERIC
Active Listing

Teva Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Ferric Citrate
NDC 0480-2996

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

Dasatinib
NDC 0480-3523

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

Dasatinib
NDC 0480-3524

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

Pazopanib
NDC 0480-4184

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

Dasatinib
NDC 0480-5101

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

Dasatinib
NDC 0480-5102

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

Dasatinib
NDC 0480-5103

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

Dasatinib
NDC 0480-5104

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

Tiopronin
NDC 0480-7824

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

Tiopronin
NDC 0480-9227

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

Alyq
NDC 0480-9277

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

Upsher-Smith Laboratories, LLC

NDC Product
Human Prescription Drug

Qudexy Xr
NDC 0245-1071

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

Qudexy Xr
NDC 0245-1072

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

Qudexy Xr
NDC 0245-1073

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

Qudexy Xr
NDC 0245-1074

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

Qudexy Xr
NDC 0245-1075

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

WALGREEN CO

NDC Product
Human Otc Drug

Acetaminophen Aspirin Caffeine
NDC 0363-9680

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

WALGREEN CO.

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 0363-0361

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

Ibuprofen And Pseudoephedrine Hcl
NDC 0363-1106

Generic Name
Ibuprofen And Pseudoephedrine Hcl
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing

WALGREENS

NDC Product
Human Otc Drug

Acetaminophen
NDC 0363-9992

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

WALGREENS CO.

NDC Product
Human Otc Drug

Acetaminophen
NDC 0363-9993

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

Walgreens

NDC Product
Human Otc Drug

Acetaminophen
NDC 0363-0892

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

Walgreens Company

NDC Product
Human Otc Drug

Fexofenadine Hydrochloride
NDC 0363-0783

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

Wal-fex
NDC 0363-0784

Generic Name
Fexofenadine Hydrochloride
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 0008-0841

Generic Name
Pantoprazole Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Protonix Delayed-release
NDC 0008-0843

Generic Name
Pantoprazole Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
NDA
Active Listing
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
NDC Product
Human Prescription Drug

Premarin
NDC 0046-1100

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

Premarin
NDC 0046-1101

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

Premarin
NDC 0046-1102

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

Premarin
NDC 0046-1103

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

Premarin
NDC 0046-1104

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

Prempro
NDC 0046-1105

Generic Name
Conjugated Estrogens And Medroxyprogesterone Acetate
Dosage Form
Tablet, Sugar Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Prempro
NDC 0046-1106

Generic Name
Conjugated Estrogens And Medroxyprogesterone Acetate
Dosage Form
Tablet, Sugar Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Prempro
NDC 0046-1107

Generic Name
Conjugated Estrogens And Medroxyprogesterone Acetate
Dosage Form
Tablet, Sugar Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Prempro
NDC 0046-1108

Generic Name
Conjugated Estrogens And Medroxyprogesterone Acetate
Dosage Form
Tablet, Sugar Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Premphase
NDC 0046-2575

Generic Name
Conjugated Estrogens And Medroxyprogesterone Acetate
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing

External Clinical & Regulatory Resources

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