HYPROMELLOSE 2208 (3 MPA.S)
UNII 9H4L916OBU

Substance Identification & Data

This profile provides standardized clinical and technical data for Hypromellose 2208 (3 Mpa.s), uniquely identified by the FDA Unique Ingredient Identifier (UNII) 9H4L916OBU.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9004-65-3 and the RxNorm Concept ID (RxCUI) 1300446. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
9H4L916OBU
CAS Registry Number
9004-65-3
RxNorm Concept ID
1300446

Detailed Substance Profile

Preferred Name
HYPROMELLOSE 2208 (3 MPA.S)
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
9H4L916OBU
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 2208 (3 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 2208 (3 CPS)
HYPROMELLOSE 2208 (3 CPS)
HYPROMELLOSE 2208 (3 MPA.S)

Brand / Trade Names

METHOCEL K3
METHOCEL K3 PREMIUM

NDC Products Containing HYPROMELLOSE 2208 (3 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 (131), only Active Listings are currently displayed.
→ A-S Medication Solutions 5
→ ANI Pharmaceuticals, Inc. 1
→ Albertsons Companies 1
→ American Health Packaging 1
→ Amneal Pharmaceuticals NY LLC 5
→ Aurobindo Pharma Limited 3
→ Biocon Pharma Inc. 4
→ Bryant Ranch Prepack 4
→ CVS Health Corp. 1
→ Camber Pharmaceuticals, Inc. 1
→ Chain Drug Consortium, LLC 1
→ Chain Drug Marketing Association 2
→ Discount Drug Mart, Inc 1
→ Dr. Reddy's Laboratories Inc. 1
→ Dr. Reddy's Laboratories Limited 2
→ Dr.Reddys Laboratories Inc 4
→ Eisai Inc. 3
→ Gericare Pharmaceuticals 1
→ H2-Pharma, LLC 1
→ HEB 1
→ Jubilant Cadista Pharmaceuticals Inc. 3
→ KVK-Tech, Inc. 3
→ LEADER/ Cardinal Health 110, Inc. 1
→ Lifestar Pharma LLC 2
→ Lupin Pharmaceuticals, Inc. 1
→ Micro Labs Limited 2
→ NorthStar Rx LLC 1
→ NorthStar RxLLC 4
→ Northstar Rx LLC 3
→ PD-Rx Pharmaceuticals, Inc. 7
→ Preferred Pharmaceuticals Inc. 1
→ Preferred Pharmaceuticals, Inc. 1
→ Proficient Rx LP 4
→ REMEDYREPACK INC. 4
→ RUGBY LABORATORIES 1
→ Sandoz Inc 2
→ Teva Pharmaceuticals USA, Inc. 21
→ Teva Pharmaceuticals, Inc. 1
→ Teyro Labs Private Limited 2
→ The Kroger Co. 1
→ Umedica Laboratories USA Inc. 3
→ Upsher-Smith Laboratories, LLC 4
→ Wal-Mart Stores Inc 1
→ Walgreens Company 1

A-S Medication Solutions

NDC Product
Human Prescription Drug

Kelnor 1/35
NDC 50090-2191

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

Ezetimibe
NDC 50090-3422

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

Ezetimibe
NDC 50090-6630

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

Ezetimibe
NDC 50090-6631

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

Ezetimibe
NDC 50090-7099

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

ANI Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Tranexamic Acid
NDC 62559-265

Generic Name
Tranexamic Acid
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Albertsons Companies

NDC Product
Human Otc Drug

Omeprazole Magnesium
NDC 21130-398

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

American Health Packaging

NDC Product
Human Prescription Drug

Tranexamic Acid
NDC 60687-750

Generic Name
Tranexamic Acid
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Amneal Pharmaceuticals NY LLC

NDC Product
Human Prescription Drug

Everolimus
NDC 60219-2279

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

Everolimus
NDC 60219-2280

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

Everolimus
NDC 60219-2281

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

Deferasirox
NDC 69238-1486

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

Deferasirox
NDC 69238-1488

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

Aurobindo Pharma Limited

NDC Product
Human Prescription Drug

Ezetimibe
NDC 59651-052

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

Pantoprazole Sodium
NDC 59651-671

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

Tranexamic Acid
NDC 59651-839

Generic Name
Tranexamic Acid
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Biocon Pharma Inc.

NDC Product
Human Prescription Drug

Everolimus
NDC 70377-010

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

Everolimus
NDC 70377-011

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

Everolimus
NDC 70377-012

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

Everolimus
NDC 70377-013

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

Bryant Ranch Prepack

NDC Product
Human Prescription Drug

Carbamazepine
NDC 63629-5914

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

Tranexamic Acid
NDC 71335-1981

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

Ezetimibe
NDC 71335-2123

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

Hydroxyzine Hydrochloride
NDC 71335-2451

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

CVS Health Corp.

NDC Product
Human Otc Drug

Omeprazole Magnesium
NDC 69842-027

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

Camber Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Pantoprazole Sodium
NDC 31722-032

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

Chain Drug Consortium, LLC

NDC Product
Human Otc Drug

Omeprazole Magnesium
NDC 68016-760

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

Chain Drug Marketing Association

NDC Product
Human Otc Drug

Omeprazole Magnesium
NDC 63868-177

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

Omeprazole Magnesium
NDC 83324-117

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

Discount Drug Mart, Inc

NDC Product
Human Otc Drug

Omeprazole Magnesium
NDC 53943-520

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

Dr. Reddy's Laboratories Inc.

NDC Product
Human Otc Drug

Omeprazole Magnesium
NDC 43598-813

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

Dr. Reddy's Laboratories Limited

NDC Product
Human Otc Drug

Omeprazole Magnesium
NDC 55111-397

Generic Name
Omeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 55111-397

Generic Name
Omeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing

Dr.Reddys Laboratories Inc

Eisai Inc.

NDC Product
Human Prescription Drug

Banzel
NDC 62856-582

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

Banzel
NDC 62856-583

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

Banzel
NDC 62856-584

Generic Name
Rufinamide
Dosage Form
Suspension
Route
Oral
Marketing
NDA
Active Listing

Gericare Pharmaceuticals

NDC Product
Human Otc Drug

Omeprazole Magnesium
NDC 57896-759

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

H2-Pharma, LLC

NDC Product
Human Prescription Drug

Xeloda
NDC 61269-475

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

HEB

NDC Product
Human Otc Drug

Omeprazole Magnesium
NDC 37808-006

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

Jubilant Cadista Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Carbamazepine
NDC 59746-789

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

Carbamazepine
NDC 59746-790

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

Carbamazepine
NDC 59746-791

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

KVK-Tech, Inc.

NDC Product
Human Prescription Drug

Hydroxyzine Hydrochloride
NDC 10702-010

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

Hydroxyzine Hydrochloride
NDC 10702-011

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

Hydroxyzine Hydrochloride
NDC 10702-012

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

LEADER/ Cardinal Health 110, Inc.

NDC Product
Human Otc Drug

Acid Reducer
NDC 70000-0232

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

Lifestar Pharma LLC

NDC Product
Human Prescription Drug

Capecitabine
NDC 70756-815

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

Capecitabine
NDC 70756-816

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

Lupin Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Nabumetone
NDC 68180-142

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

Micro Labs Limited

NDC Product
Human Prescription Drug

Rufinamide
NDC 42571-391

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

Rufinamide
NDC 42571-392

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

NorthStar Rx LLC

NDC Product
Human Prescription Drug

Ezetimibe
NDC 16714-813

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

NorthStar RxLLC

NDC Product
Human Prescription Drug

Everolimus
NDC 72603-254

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

Everolimus
NDC 72603-255

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

Everolimus
NDC 72603-256

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

Everolimus
NDC 72603-257

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

Northstar Rx LLC

NDC Product
Human Prescription Drug

Carbamazepine
NDC 72603-886

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

Carbamazepine
NDC 72603-887

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

Carbamazepine
NDC 72603-888

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

PD-Rx Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Hydroxyzine Hydrochloride
NDC 43063-518

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

Hydroxyzine Hydrochloride
NDC 43063-519

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

Hydroxyzine Hydrochloride
NDC 43063-943

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

Hydroxyzine Hydrochloride
NDC 43063-960

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

Hydroxyzine Hydrochloride
NDC 43063-962

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

Hydroxyzine Hydrochloride
NDC 43063-963

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

Norgestimate And Ethinyl Estradiol
NDC 72789-434

Generic Name
Norgestimate And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing

Preferred Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Tri-sprintec
NDC 68788-6325

Generic Name
Norgestimate And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing

Preferred Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Sprintec
NDC 68788-7429

Generic Name
Norgestimate And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing

Proficient Rx LP

NDC Product
Human Prescription Drug

Tri-sprintec
NDC 63187-458

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

Sprintec
NDC 63187-911

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

Tri-lo-sprintec
NDC 71205-287

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

Ezetimibe
NDC 82804-064

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

REMEDYREPACK INC.

NDC Product
Human Prescription Drug

Hydroxyzine Hydrochloride
NDC 70518-1730

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

Carbamazepine
NDC 70518-3699

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

Carbamazepine
NDC 70518-3773

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

Carbamazepine
NDC 70518-3911

Generic Name
Carbamazepine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
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

Sandoz Inc

NDC Product
Human Prescription Drug

Dapagliflozin
NDC 0781-5985

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

Dapagliflozin
NDC 0781-5990

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

Teva Pharmaceuticals USA, Inc.

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

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

Dexmethylphenidate Hydrochloride
NDC 0093-5045

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

Dexmethylphenidate Hydrochloride
NDC 0093-5046

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

Methylphenidate Hydrochloride (la)
NDC 0093-5346

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

Methylphenidate Hydrochloride (la)
NDC 0093-5347

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

Methylphenidate Hydrochloride (la)
NDC 0093-5348

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

Dexmethylphenidate Hydrochloride
NDC 0093-5550

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

Dexmethylphenidate Hydrochloride
NDC 0093-5551

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

Dexmethylphenidate Hydrochloride
NDC 0093-5552

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

Dexmethylphenidate Hydrochloride
NDC 0093-5553

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

Dexmethylphenidate Hydrochloride
NDC 0093-5554

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

Dexmethylphenidate Hydrochloride
NDC 0093-5562

Generic Name
Dexmethylphenidate Hydrochloride
Dosage Form
Capsule, Extended Release
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
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

Sprintec
NDC 0555-9016

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

Tri-sprintec
NDC 0555-9018

Generic Name
Norgestimate 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

Kelnor 1/35
NDC 0555-9064

Generic Name
Ethynodiol Diacetate 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

Vestura
NDC 0480-4000

Generic Name
Drospirenone And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing

Teyro Labs Private Limited

NDC Product
Human Prescription Drug

Capecitabine
NDC 82511-001

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

Capecitabine
NDC 82511-002

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

The Kroger Co.

NDC Product
Human Otc Drug

Omeprazole Magnesium
NDC 30142-012

Generic Name
Omeprazole Magnesium 20.6mg Capsules
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Umedica Laboratories USA Inc.

NDC Product
Human Prescription Drug

Carbamazepine
NDC 60290-058

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

Carbamazepine
NDC 60290-059

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

Carbamazepine
NDC 60290-060

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

Upsher-Smith Laboratories, LLC

NDC Product
Human Prescription Drug

Torpenz
NDC 0245-0822

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

Torpenz
NDC 0245-0823

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

Torpenz
NDC 0245-0824

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

Torpenz
NDC 0245-0825

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

Wal-Mart Stores Inc

NDC Product
Human Otc Drug

Omeprazole Magnesium
NDC 49035-397

Generic Name
Omeprazole Magnesium 20.6mg Capsules
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Walgreens Company

NDC Product
Human Otc Drug

Omeprazole Magnesium
NDC 0363-0042

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

External Clinical & Regulatory Resources

CAS
Common Chemistry
NCATS
Inxight Drugs
NLM
DailyMed Products
NCATS
GSRS Full Record