POLYETHYLENE OXIDE 200000
UNII 11628IH70O

Substance Identification & Data

This profile provides standardized clinical and technical data for Polyethylene Oxide 200000, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 11628IH70O.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 25322-68-3 and the RxNorm Concept ID (RxCUI) 1809901. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
11628IH70O
CAS Registry Number
25322-68-3
RxNorm Concept ID
1809901

Detailed Substance Profile

Preferred Name
POLYETHYLENE OXIDE 200000
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
11628IH70O
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 Polyethylene Oxide 200000. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.

FDA Official Name

PEG-5M

Common Names & Synonyms

MACROGOL 200000
PEG 200000
POLYETHYLENE GLYCOL 200000
POLYETHYLENE GLYCOL 200000 [II]
POLYETHYLENE GLYCOL 220000
POLYETHYLENE OXIDE 200000
POLYETHYLENE OXIDE 200K

Brand / Trade Names

ALKOX R-1000G
POLYOX WSR N-80
RITA PEO 1
RITA PEO-1

NDC Products Containing POLYETHYLENE OXIDE 200000

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 (121), only Active Listings are currently displayed.
→ A-S Medication Solutions 4
→ Alembic Pharmaceuticals Inc. 3
→ Alembic Pharmaceuticals Limited 3
→ Alvogen Inc. 4
→ Amneal Pharmaceuticals NY LLC 2
→ Aquestive Therapeutics 3
→ Archis Pharma LLC 3
→ Bryant Ranch Prepack 4
→ Camber Pharmaceuticals, Inc 4
→ Camber Pharmaceuticals, Inc. 4
→ Dermalogica, LLC. 1
→ Eskayef Pharmaceuticals Limited 4
→ Golden State Medical Supply, Inc. 4
→ Mylan Pharmaceuticals Inc. 2
→ Northstar Rx LLC 1
→ Northwind Health Company, LLC 2
→ Oryza pharmaceuticals Inc. 3
→ PD-Rx Pharmaceuticals, Inc. 1
→ Preferred Pharmaceuticals Inc. 2
→ Proficient Rx LP 1
→ REMEDYREPACK INC. 5
→ Redpharm Drug 1
→ Rising Pharma Holdings, Inc. 6
→ Slate Run Pharmaceuticals, LLC 6
→ Sun Pharmaceutical Industries, Inc. 5
→ Trigen Laboratories, LLC 11
→ Tris Pharma Inc 4
→ Vertical Pharmaceuticals, LLC 2
→ Westminster Pharmaceuticals, LLC 4
→ XLCare Pharmaceuticals, Inc. 4
→ Zhejiang Jutai Pharamceutical Co., Ltd 3
→ Zydus Lifesciences Limited 2
→ Zydus Pharmaceuticals (USA) Inc. 2

A-S Medication Solutions

NDC Product
Human Prescription Drug

Glipizide
NDC 50090-5040

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

Glipizide
NDC 50090-5806

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

Oxybutynin Chloride Extended Release
NDC 50090-6673

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

Oxybutynin Chloride Extended Release
NDC 50090-6840

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

Alembic Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Nifedipine
NDC 62332-732

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

Nifedipine
NDC 62332-733

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

Nifedipine
NDC 62332-734

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

Alembic Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Nifedipine
NDC 46708-732

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

Nifedipine
NDC 46708-733

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

Nifedipine
NDC 46708-734

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

Alvogen Inc.

Amneal Pharmaceuticals NY LLC

NDC Product
Human Prescription Drug

Mirabegron
NDC 69238-2860

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

Mirabegron
NDC 69238-2861

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

Aquestive Therapeutics

NDC Product
Human Prescription Drug

Sympazan
NDC 10094-205

Generic Name
Clobazam
Dosage Form
Film
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Sympazan
NDC 10094-210

Generic Name
Clobazam
Dosage Form
Film
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Sympazan
NDC 10094-220

Generic Name
Clobazam
Dosage Form
Film
Route
Oral
Marketing
NDA
Active Listing

Archis Pharma LLC

NDC Product
Human Prescription Drug

Paliperidone
NDC 72819-158

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

Paliperidone
NDC 72819-159

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

Paliperidone
NDC 72819-160

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

Bryant Ranch Prepack

NDC Product
Human Prescription Drug

Glipizide
NDC 71335-1031

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

Glipizide
NDC 71335-1042

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

Oxybutynin Chloride Extended Release
NDC 71335-2121

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

Oxybutynin Chloride Extended Release
NDC 71335-2330

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

Camber Pharmaceuticals, Inc

NDC Product
Human Prescription Drug

Paliperidone
NDC 31722-317

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

Paliperidone
NDC 31722-318

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

Paliperidone
NDC 31722-319

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

Paliperidone
NDC 31722-320

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

Camber Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Hydromorphone Hydrochloride
NDC 31722-119

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

Hydromorphone Hydrochloride
NDC 31722-120

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

Hydromorphone Hydrochloride
NDC 31722-121

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

Hydromorphone Hydrochloride
NDC 31722-122

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

Dermalogica, LLC.

NDC Product
Human Otc Drug

Porescreen Spf40
NDC 68479-291

Generic Name
Zinc Oxide
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Eskayef Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Paliperidone
NDC 72658-1253

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

Paliperidone
NDC 72658-1254

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

Paliperidone
NDC 72658-1255

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

Paliperidone
NDC 72658-1256

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

Golden State Medical Supply, Inc.

NDC Product
Human Prescription Drug

Methylphenidate Hydrochloride
NDC 51407-924

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

Methylphenidate Hydrochloride
NDC 51407-925

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

Methylphenidate Hydrochloride
NDC 51407-926

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

Methylphenidate Hydrochloride
NDC 51407-927

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

Mylan Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Buprenorphine And Naloxone
NDC 0378-8767

Generic Name
Buprenorphine And Naloxone
Dosage Form
Film
Route
Buccal; Sublingual
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Buprenorphine And Naloxone
NDC 0378-8768

Generic Name
Buprenorphine And Naloxone
Dosage Form
Film
Route
Buccal; Sublingual
Marketing
ANDA
Active Listing

Northstar Rx LLC

NDC Product
Human Prescription Drug

Methylphenidate Hydrochloride
NDC 72603-399

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

Northwind Health Company, LLC

NDC Product
Human Prescription Drug

Glipizide
NDC 51655-337

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

Glipizide
NDC 51655-966

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

Oryza pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 72516-026

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

Metoprolol Succinate
NDC 72516-027

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

Metoprolol Succinate
NDC 72516-028

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

PD-Rx Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Oxybutynin Chloride Extended Release
NDC 72789-414

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

Preferred Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Glipizide
NDC 68788-7856

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

Glipizide
NDC 68788-8487

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

Proficient Rx LP

NDC Product
Human Prescription Drug

Oxybutynin Chloride Extended Release
NDC 82804-095

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

REMEDYREPACK INC.

NDC Product
Human Prescription Drug

Glipizide
NDC 70518-1063

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

Glipizide
NDC 70518-1848

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

Glipizide
NDC 70518-2308

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

Mirabegron
NDC 70518-4304

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

Mirabegron
NDC 70518-4631

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

Redpharm Drug

Rising Pharma Holdings, Inc.

NDC Product
Human Prescription Drug

Oxybutynin Chloride Extended Release
NDC 64980-209

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

Oxybutynin Chloride Extended Release
NDC 64980-210

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

Oxybutynin Chloride Extended Release
NDC 64980-211

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

Glipizide
NDC 64980-279

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

Glipizide
NDC 64980-280

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

Glipizide
NDC 64980-281

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

Slate Run Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 70436-195

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

Diltiazem Hydrochloride
NDC 70436-196

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

Diltiazem Hydrochloride
NDC 70436-197

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

Diltiazem Hydrochloride
NDC 70436-198

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

Diltiazem Hydrochloride
NDC 70436-199

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

Diltiazem Hydrochloride
NDC 70436-200

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

Sun Pharmaceutical Industries, Inc.

NDC Product
Human Prescription Drug

Methylphenidate Hydrochloride
NDC 57664-606

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

Methylphenidate Hydrochloride
NDC 57664-607

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

Methylphenidate Hydrochloride
NDC 57664-608

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

Methylphenidate Hydrochloride
NDC 57664-609

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

Methylphenidate Hydrochloride
NDC 57664-710

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

Trigen Laboratories, LLC

NDC Product
Human Prescription Drug

Methylphenidate Hydrochloride
NDC 13811-700

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

Methylphenidate Hydrochloride
NDC 13811-706

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

Methylphenidate Hydrochloride
NDC 13811-707

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

Methylphenidate Hydrochloride
NDC 13811-708

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

Methylphenidate Hydrochloride
NDC 13811-709

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

Methylphenidate Hydrochloride
NDC 13811-710

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

Methylphenidate Hydrochloride
NDC 13811-711

Generic Name
Methylphenidate Hydrochloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing

Tris Pharma Inc

NDC Product
Human Prescription Drug

Paliperidone
NDC 27808-222

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

Paliperidone
NDC 27808-223

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

Paliperidone
NDC 27808-224

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

Paliperidone
NDC 27808-225

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

Vertical Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Relexxii
NDC 68025-088

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

Relexxii
NDC 68025-089

Generic Name
Methylphenidate Hydrochloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
NDA
Active Listing

Westminster Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Paliperidone
NDC 69367-432

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

Paliperidone
NDC 69367-433

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

Paliperidone
NDC 69367-434

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

Paliperidone
NDC 69367-435

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

XLCare Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Hydromorphone Hydrochloride
NDC 72865-168

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

Hydromorphone Hydrochloride
NDC 72865-169

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

Hydromorphone Hydrochloride
NDC 72865-170

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

Hydromorphone Hydrochloride
NDC 72865-171

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

Zhejiang Jutai Pharamceutical Co., Ltd

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 71765-006

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

Metoprolol Succinate
NDC 71765-007

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

Metoprolol Succinate
NDC 71765-008

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

Zydus Lifesciences Limited

NDC Product
Human Prescription Drug

Mirabegron
NDC 70771-1752

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

Mirabegron
NDC 70771-1753

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

Zydus Pharmaceuticals (USA) Inc.

NDC Product
Human Prescription Drug

Mirabegron
NDC 70710-1159

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

Mirabegron
NDC 70710-1160

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

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