ETHYL ACRYLATE AND METHYL METHACRYLATE COPOLYMER (2:1; 750000 MW)
UNII P2OM2Q86BI

Substance Identification & Data

This profile provides standardized clinical and technical data for Ethyl Acrylate And Methyl Methacrylate Copolymer (2:1; 750000 Mw), uniquely identified by the FDA Unique Ingredient Identifier (UNII) P2OM2Q86BI.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9010-88-2 and the RxNorm Concept ID (RxCUI) 1426457. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
P2OM2Q86BI
CAS Registry Number
9010-88-2
RxNorm Concept ID
1426457

Detailed Substance Profile

Preferred Name
ETHYL ACRYLATE AND METHYL METHACRYLATE COPOLYMER (2:1; 750000 MW)
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
P2OM2Q86BI
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 Ethyl Acrylate And Methyl Methacrylate Copolymer (2:1; 750000 Mw). 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

ETHYL ACRYLATE - METHYL METHACRYLATE COPOLYMER
ETHYL ACRYLATE AND METHYL METHACRYLATE COPOLYMER
ETHYL ACRYLATE AND METHYL METHACRYLATE COPOLYMER (2:1; 750000 MW)
ETHYL ACRYLATE AND METHYL METHACRYLATE COPOLYMER (2:1; 750000 MW) [II]

NDC Products Containing ETHYL ACRYLATE AND METHYL METHACRYLATE COPOLYMER (2:1; 750000 MW)

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 (130), only Active Listings are currently displayed.
→ A-S Medication Solutions 2
→ Alembic Pharmaceuticals Inc. 1
→ Alembic Pharmaceuticals Limited 1
→ American Health Packaging 1
→ Ascend Laboratories, LLC 1
→ AvPAK 1
→ Bausch Health US LLC 11
→ Bausch Health US, LLC 6
→ Bryant Ranch Prepack 9
→ DIRECT RX 1
→ Direct_Rx 1
→ Evofem Inc. 1
→ Guangzhou Fantesy Biotechnology Co.,Ltd 1
→ Jubilant Cadista Pharmaceuticals Inc. 3
→ Lupin Pharmaceuticals, Inc. 2
→ NCS HealthCare of KY, LLC dba Vangard Labs 2
→ Northstar Rx LLC 3
→ NuCare Pharmaceuticals,Inc. 3
→ OCEANSIDE PHARMACEUTICALS 4
→ Oceanside Pharmaceuticals 11
→ PD-Rx Pharmaceuticals, Inc. 1
→ Preferred Pharmaceuticals Inc. 1
→ Preferred Pharmaceuticals, Inc. 1
→ REMEDYREPACK INC. 5
→ Sandoz Inc 1
→ Slate Run Pharmaceuticals, LLC 6
→ Trigen Laboratories, LLC 3
→ Umedica Laboratories USA Inc. 3
→ Vertical Pharmaceuticals, LLC 3
→ Zydus Lifesciences Limited 3
→ Zydus Pharmaceuticals USA Inc. 3
→ direct rx 1

A-S Medication Solutions

NDC Product
Human Prescription Drug

Venlafaxine Hydrochloride
NDC 50090-6301

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

Diltiazem Hydrochloride
NDC 50090-7815

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

Alembic Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Mesalamine
NDC 62332-724

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

Alembic Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Mesalamine
NDC 46708-724

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

American Health Packaging

NDC Product
Human Prescription Drug

Mesalamine
NDC 60687-650

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

Ascend Laboratories, LLC

NDC Product
Human Prescription Drug

Mesalamine
NDC 67877-717

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

AvPAK

NDC Product
Human Prescription Drug

Mesalamine
NDC 50268-577

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

Bausch Health US LLC

NDC Product
Human Prescription Drug

Cardizem Cd
NDC 0187-0795

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

Cardizem Cd
NDC 0187-0796

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

Cardizem Cd
NDC 0187-0797

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

Cardizem Cd
NDC 0187-0798

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

Cardizem Cd
NDC 0187-0799

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

Cardizem La
NDC 0187-2045

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

Cardizem La
NDC 0187-2046

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

Cardizem La
NDC 0187-2047

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

Cardizem La
NDC 0187-2048

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

Cardizem La
NDC 0187-2049

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

Cardizem La
NDC 0187-2050

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

Bausch Health US, LLC

NDC Product
Human Prescription Drug

Tiazac Extended Release
NDC 0187-2612

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

Tiazac Extended Release
NDC 0187-2613

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

Tiazac Extended Release
NDC 0187-2614

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

Tiazac Extended Release
NDC 0187-2615

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

Tiazac Extended Release
NDC 0187-2616

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

Tiazac Extended Release
NDC 0187-2617

Generic Name
Diltiazem Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA
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

Diltiazem Hydrochloride Extended Release
NDC 63629-7981

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

Diltiazem Hydrochloride
NDC 71335-0634

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

Diltiazem Hydrochloride
NDC 71335-0643

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

Diltiazem Hydrochloride
NDC 71335-0867

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

Venlafaxine Hydrochloride
NDC 71335-1338

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

Diltiazem Hydrochloride
NDC 71335-1389

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

Diltiazem Hydrochloride Extended Release
NDC 71335-1585

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

Divalproex Sodium
NDC 71335-1883

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

DIRECT RX

Direct_Rx

NDC Product
Human Prescription Drug

Divalproex Sodium Er
NDC 72189-459

Generic Name
Divalproex Sodium Er
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Evofem Inc.

NDC Product
Human Prescription Drug

Solosec
NDC 69751-400

Generic Name
Secnidazole
Dosage Form
Granule
Route
Oral
Marketing
NDA
Active Listing

Guangzhou Fantesy Biotechnology Co.,Ltd

NDC Product
Human Otc Drug

Orlaskin Hydrating Sunscreen
NDC 83447-003

Generic Name
Orlaskin Hydrating Sunscreen
Dosage Form
Spray
Route
Cutaneous
Marketing
OTC MONOGRAPH DRUG
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

Lupin Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 68180-260

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

Divalproex Sodium
NDC 68180-261

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

NCS HealthCare of KY, LLC dba Vangard Labs

NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 0615-8376

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

Divalproex Sodium
NDC 0615-8377

Generic Name
Divalproex Sodium
Dosage Form
Tablet, Extended Release
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

NuCare Pharmaceuticals,Inc.

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 68071-4005

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

Venlafaxine Hydrochloride
NDC 68071-4442

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

Diltiazem Hydrochloride
NDC 68071-4664

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

OCEANSIDE PHARMACEUTICALS

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 68682-993

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

Diltiazem Hydrochloride
NDC 68682-994

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

Diltiazem Hydrochloride
NDC 68682-997

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

Diltiazem Hydrochloride
NDC 68682-998

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

Oceanside Pharmaceuticals

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride Extended Release
NDC 68682-367

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

Diltiazem Hydrochloride Extended Release
NDC 68682-368

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

Diltiazem Hydrochloride Extended Release
NDC 68682-369

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

Diltiazem Hydrochloride Extended Release
NDC 68682-370

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

Diltiazem Hydrochloride Extended Release
NDC 68682-371

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

Diltiazem Hydrochloride Extended Release
NDC 68682-372

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

Diltiazem Hydrochloride
NDC 68682-705

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

Diltiazem Hydrochloride
NDC 68682-706

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

Diltiazem Hydrochloride
NDC 68682-707

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

Diltiazem Hydrochloride
NDC 68682-708

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

Diltiazem Hydrochloride
NDC 68682-709

Generic Name
Diltiazem Hydrochloride Extended-release Tablets
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing

PD-Rx Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 72789-286

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

Preferred Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Venlafaxine Hydrochloride
NDC 68788-6806

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

Preferred Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 68788-8358

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

REMEDYREPACK INC.

NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 70518-3183

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

Divalproex Sodium
NDC 70518-3477

Generic Name
Divalproex Sodium
Dosage Form
Tablet, Extended Release
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

Sandoz Inc

NDC Product
Human Prescription Drug

Tamsulosin Hydrochloride
NDC 0781-2076

Generic Name
Tamsulosin Hydrochloride
Dosage Form
Capsule
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

Trigen Laboratories, LLC

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

Vertical Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Conzip
NDC 68025-071

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

Conzip
NDC 68025-072

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

Conzip
NDC 68025-073

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

Zydus Lifesciences Limited

NDC Product
Human Prescription Drug

Venlafaxine Hydrochloride
NDC 65841-751

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

Venlafaxine Hydrochloride
NDC 65841-752

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

Venlafaxine Hydrochloride
NDC 65841-753

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

Zydus Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Venlafaxine Hydrochloride
NDC 68382-034

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

Venlafaxine Hydrochloride
NDC 68382-035

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

Venlafaxine Hydrochloride
NDC 68382-036

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

direct rx

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride Extended Release
NDC 72189-248

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

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