NDC Product
Human Prescription DrugSprycel NDC 0003-0524
- Generic Name
- Dasatinib
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Magnesium Stearate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 70097M6I30.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 557-04-0 and the RxNorm Concept ID (RxCUI) 1310567. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
MAGNESIUM STEARATE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
70097M6I30
The specific atomic composition represented as a molecular structure string.
InChIKey
2C18H35O2.Mg International Chemical Identifier digital signature for unique molecular identification.
SMILES String
HQKMJHAJHXVSDF-UHFFFAOYSA-L Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
C(=O)([O-])CCCCCCCCCCCCCCCCC.[Mg+2].C(=O)([O-])CCCCCCCCCCCCCCCCC
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Magnesium Stearate. 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
MAGNESIUM STEARATE
OF
Common Names & Synonyms
DIBASIC MAGNESIUM STEARATE
CN
MAGNESII STEARAS [WHO-IP LATIN]
CN
MAGNESIUM STEARATE [HSDB]
CN
MAGNESIUM STEARATE [II]
CN
MAGNESIUM STEARATE [JAN]
CN
MAGNESIUM STEARATE [MI]
CN
MAGNESIUM STEARATE [VANDF]
CN
MAGNESIUM STEARATE [WHO-DD]
CN
MAGNESIUM STEARATE G
CN
OCTADECANOIC ACID, MAGNESIUM SALT (2:1)
CN
Systematic Nomenclature
MAGNESIUM DISTEARATE
SYS
MAGNESIUM OCTADECANOATE
SYS
NDC Products Containing MAGNESIUM STEARATE
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.
Showing 200 active products
E.R. Squibb & Sons, L.L.C.
Active Listing
NDC Product
Human Prescription DrugSprycel NDC 0003-0527
- Generic Name
- Dasatinib
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSprycel NDC 0003-0528
- Generic Name
- Dasatinib
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSprycel NDC 0003-0852
- Generic Name
- Dasatinib
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSprycel NDC 0003-0855
- Generic Name
- Dasatinib
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSprycel NDC 0003-0857
- Generic Name
- Dasatinib
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugEliquis NDC 0003-0893
- Generic Name
- Apixaban
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugEliquis NDC 0003-0894
- Generic Name
- Apixaban
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSotyktu NDC 0003-0895
- Generic Name
- Deucravacitinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBaraclude NDC 0003-1611
- Generic Name
- Entecavir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBaraclude NDC 0003-1612
- Generic Name
- Entecavir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBaraclude NDC 0003-1614
- Generic Name
- Entecavir
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugReyataz NDC 0003-3622
- Generic Name
- Atazanavir
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugReyataz NDC 0003-3631
- Generic Name
- Atazanavir
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugReyataz NDC 0003-3638
- Generic Name
- Atazanavir
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugEvotaz NDC 0003-3641
- Generic Name
- Atazanavir And Cobicistat
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugEliquis 30-day Starter Pack NDC 0003-3764
- Generic Name
- Apixaban
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
Eli Lilly and Company
NDC Product
Human Prescription DrugInluriyo NDC 0002-1717
- Generic Name
- Imlunestrant
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFoundayo NDC 0002-4178
- Generic Name
- Orforglipron
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugOlumiant NDC 0002-4182
- Generic Name
- Baricitinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugEvista NDC 0002-4184
- Generic Name
- Raloxifene Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugReyvow NDC 0002-4312
- Generic Name
- Lasmiditan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCialis NDC 0002-4462
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCialis NDC 0002-4463
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCialis NDC 0002-4464
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugReyvow NDC 0002-4491
- Generic Name
- Lasmiditan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFoundayo NDC 0002-4503
- Generic Name
- Orforglipron
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugOlumiant NDC 0002-4732
- Generic Name
- Baricitinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFoundayo NDC 0002-4794
- Generic Name
- Orforglipron
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFoundayo NDC 0002-4803
- Generic Name
- Orforglipron
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFoundayo NDC 0002-4839
- Generic Name
- Orforglipron
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFoundayo NDC 0002-4953
- Generic Name
- Orforglipron
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBaricitinib NDC 0002-6885
- Generic Name
- Baricitinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- EMERGENCY USE AUTHORIZATION
Active Listing
NDC Product
Human Prescription DrugJaypirca NDC 0002-6902
- Generic Name
- Pirtobrutinib
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugJaypirca NDC 0002-7026
- Generic Name
- Pirtobrutinib
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Genentech, Inc.
NDC Product
Human Prescription DrugCellcept NDC 0004-0259
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCellcept NDC 0004-0260
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCellcept NDC 0004-0261
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCellcept NDC 0004-0298
- Generic Name
- Mycophenolate Mofetil Hydrochloride
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA Inc
NDC Product
Human Prescription DrugImipramine Pamoate NDC 0054-0273
- Generic Name
- Imipramine Pamoate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImipramine Pamoate NDC 0054-0274
- Generic Name
- Imipramine Pamoate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImipramine Pamoate NDC 0054-0275
- Generic Name
- Imipramine Pamoate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImipramine Pamoate NDC 0054-0276
- Generic Name
- Imipramine Pamoate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFebuxostat NDC 0054-0413
- Generic Name
- Febuxostat
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFebuxostat NDC 0054-0414
- Generic Name
- Febuxostat
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVigabatrin NDC 0054-0652
- Generic Name
- Vigabatrin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrucalopride NDC 0054-0749
- Generic Name
- Prucalopride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrucalopride 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 DrugFlecainide Acetate NDC 0054-0010
- Generic Name
- Flecainide Acetate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFlecainide Acetate NDC 0054-0011
- Generic Name
- Flecainide Acetate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFlecainide Acetate NDC 0054-0012
- Generic Name
- Flecainide Acetate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-0017
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-0018
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-0019
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLithium Carbonate NDC 0054-0020
- Generic Name
- Lithium Carbonate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTorsemide NDC 0054-0077
- Generic Name
- Torsemide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBalsalazide Disodium NDC 0054-0079
- Generic Name
- Balsalazide Disodium
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZaleplon NDC 0054-0084
- Generic Name
- Zaleplon
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZaleplon NDC 0054-0085
- Generic Name
- Zaleplon
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCalcium Acetate NDC 0054-0088
- Generic Name
- Calcium Acetate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGalantamine Hydrobromide NDC 0054-0137
- Generic Name
- Galantamine Hydrobromide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcarbose NDC 0054-0140
- Generic Name
- Acarbose
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcarbose NDC 0054-0141
- Generic Name
- Acarbose
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcarbose NDC 0054-0142
- Generic Name
- Acarbose
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMycophenolate Mofetil NDC 0054-0163
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMycophenolate Mofetil NDC 0054-0166
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBuprenorphine NDC 0054-0176
- Generic Name
- Buprenorphine
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBuprenorphine NDC 0054-0177
- Generic Name
- Buprenorphine
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Buprenorphine Hydrochloride And Naloxone Hydrochloride Dihyd...
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Buprenorphine Hydrochloride And Naloxone Hydrochloride Dihyd...
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 0054-0220
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 0054-0221
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 0054-0222
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 0054-0223
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 0054-0229
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 0054-0230
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan And Hydrochlorothiazide NDC 0054-0254
- Generic Name
- Irbesartan And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan And Hydrochlorothiazide NDC 0054-0255
- Generic Name
- Irbesartan And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNaratriptan NDC 0054-0278
- Generic Name
- Naratriptan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNaratriptan NDC 0054-0279
- Generic Name
- Naratriptan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0054-0283
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxymorphone Hydrochloride NDC 0054-0284
- Generic Name
- Oxymorphone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCevimeline Hydrochloride NDC 0054-0334
- Generic Name
- Cevimeline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0370
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0371
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0372
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0373
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0374
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0375
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydromorphone Hydrochloride NDC 0054-0386
- Generic Name
- Hydromorphone Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethamphetamine Hydrochloride NDC 0054-0389
- Generic Name
- Methamphetamine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDesvenlafaxine NDC 0054-0400
- Generic Name
- Desvenlafaxine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDesvenlafaxine NDC 0054-0401
- Generic Name
- Desvenlafaxine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRufinamide NDC 0054-0425
- Generic Name
- Rufinamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRufinamide NDC 0054-0426
- Generic Name
- Rufinamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevorphanol Tartrate NDC 0054-0438
- Generic Name
- Levorphanol Tartrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 0054-0470
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 0054-0471
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 0054-0472
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 0054-0480
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 0054-0481
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEverolimus NDC 0054-0497
- Generic Name
- Everolimus
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDeferiprone NDC 0054-0576
- Generic Name
- Deferiprone
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDesvenlafaxine NDC 0054-0603
- Generic Name
- Desvenlafaxine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Butalbital, Acetaminophen, Caffeine And Codeine Phosphate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethadone Hydrochloride NDC 0054-0709
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethadone Hydrochloride NDC 0054-0710
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDeferiprone NDC 0054-0711
- Generic Name
- Deferiprone
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 0054-0748
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTapentadol NDC 0054-0942
- Generic Name
- Tapentadol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugTapentadol NDC 0054-0943
- Generic Name
- Tapentadol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugTapentadol NDC 0054-0945
- Generic Name
- Tapentadol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 0054-0962
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 0054-0963
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 0054-0964
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEltrombopag NDC 0054-0965
- Generic Name
- Eltrombopag Olamine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugBelsomra NDC 0006-0005
- Generic Name
- Suvorexant
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugStromectol NDC 0006-0032
- Generic Name
- Ivermectin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBelsomra NDC 0006-0033
- Generic Name
- Suvorexant
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugJanuvia NDC 0006-0112
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugJanuvia NDC 0006-0221
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsentress NDC 0006-0227
- Generic Name
- Raltegravir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugJanuvia NDC 0006-0277
- Generic Name
- Sitagliptin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBelsomra NDC 0006-0325
- Generic Name
- Suvorexant
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBelsomra NDC 0006-0335
- Generic Name
- Suvorexant
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsentress NDC 0006-0473
- Generic Name
- Raltegravir
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsentress NDC 0006-0477
- Generic Name
- Raltegravir
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZolinza NDC 0006-0568
- Generic Name
- Vorinostat
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPifeltro NDC 0006-3069
- Generic Name
- Doravirine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZepatier NDC 0006-3074
- Generic Name
- Elbasvir And Grazoprevir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPrevymis NDC 0006-3075
- Generic Name
- Letermovir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPrevymis NDC 0006-3076
- Generic Name
- Letermovir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsentress NDC 0006-3080
- Generic Name
- Raltegravir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsentress NDC 0006-3603
- Generic Name
- Raltegravir
- Dosage Form
- Granule, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPrevymis NDC 0006-5003
- Generic Name
- Letermovir
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPrevymis NDC 0006-5004
- Generic Name
- Letermovir
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugDelstrigo NDC 0006-5007
- Generic Name
- Doravirine, Lamivudine, And Tenofovir Disoproxil Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugVerquvo NDC 0006-5028
- Generic Name
- Vericiguat
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugVerquvo NDC 0006-5029
- Generic Name
- Vericiguat
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugVerquvo NDC 0006-5030
- Generic Name
- Vericiguat
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLagevrio NDC 0006-5055
- Generic Name
- Molnupiravir
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- EMERGENCY USE AUTHORIZATION
Active Listing
NDC Product
Human Prescription DrugIdvynso NDC 0006-5092
- Generic Name
- Doravirine, Islatravir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugWelireg NDC 0006-5331
- Generic Name
- Belzutifan
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSteglatro NDC 0006-5363
- Generic Name
- Ertugliflozin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSteglatro NDC 0006-5364
- Generic Name
- Ertugliflozin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSteglujan NDC 0006-5367
- Generic Name
- Ertugliflozin And Sitagliptin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSteglujan NDC 0006-5368
- Generic Name
- Ertugliflozin And Sitagliptin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSegluromet NDC 0006-5369
- Generic Name
- Ertugliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSegluromet NDC 0006-5370
- Generic Name
- Ertugliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSegluromet NDC 0006-5373
- Generic Name
- Ertugliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSegluromet NDC 0006-5374
- Generic Name
- Ertugliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugAzulfidine NDC 0013-0101
- Generic Name
- Sulfasalazine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAzulfidine En-tabs NDC 0013-0102
- Generic Name
- Sulfasalazine
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLomotil NDC 0025-0061
- Generic Name
- Diphenoxylate Hydrochloride And Atropine Sulfate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAldactone NDC 0025-1001
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAldactone NDC 0025-1031
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAldactone NDC 0025-1041
- Generic Name
- Spironolactone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugArthrotec NDC 0025-1411
- Generic Name
- Diclofenac Sodium And Misoprostol
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugArthrotec NDC 0025-1421
- Generic Name
- Diclofenac Sodium And Misoprostol
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFlagyl NDC 0025-1942
- Generic Name
- Metronidazole
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Pharmacia & Upjohn Company LLC
NDC Product
Human Prescription DrugHalcion NDC 0009-0017
- Generic Name
- Triazolam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCleocin Hydrochloride NDC 0009-0225
- Generic Name
- Clindamycin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCleocin Hydrochloride NDC 0009-0331
- Generic Name
- Clindamycin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCleocin Hydrochloride NDC 0009-0395
- Generic Name
- Clindamycin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugColestid NDC 0009-0450
- Generic Name
- Colestipol Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAromasin NDC 0009-7663
- Generic Name
- Exemestane
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
ROERIG
NDC Product
Human Prescription DrugGeodon NDC 0049-0056
- Generic Name
- Ziprasidone Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugGeodon NDC 0049-0058
- Generic Name
- Ziprasidone Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugGeodon NDC 0049-0352
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugGeodon NDC 0049-0354
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugGeodon NDC 0049-0356
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Roerig
NDC Product
Human Prescription DrugGlucotrol Xl NDC 0049-0178
- Generic Name
- Glipizide
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugVfend NDC 0049-3160
- Generic Name
- Voriconazole
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugDiflucan NDC 0049-3450
- Generic Name
- Fluconazole
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
Sanofi-Aventis U.S. LLC
NDC Product
Human Prescription DrugPrimaquine Phosphate NDC 0024-1596
- Generic Name
- Primaquine Phosphate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMultaq NDC 0024-4142
- Generic Name
- Dronedarone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFexinidazole NDC 0024-4512
- Generic Name
- Fexinidazole
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAvapro NDC 0024-5851
- Generic Name
- Irbesartan
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAvapro NDC 0024-5852
- Generic Name
- Irbesartan
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAvalide NDC 0024-5855
- Generic Name
- Irbesartan And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAvalide NDC 0024-5856
- Generic Name
- Irbesartan And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Viatris Specialty LLC
NDC Product
Human Prescription DrugEdluar NDC 0037-6010
- Generic Name
- Zolpidem Tartrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugEdluar NDC 0037-6050
- Generic Name
- Zolpidem Tartrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugUrelle NDC 0037-6321
- Generic Name
- Hyoscyamine Sulfate, Methenamine, Methylene Blue, Phenyl Sal...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugDipentum NDC 0037-6860
- Generic Name
- Olsalazine Sodium
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
NDC Product
Human Prescription DrugDuavee NDC 0008-1123
- Generic Name
- Conjugated Estrogens/bazedoxifene
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPristiq Extended-release NDC 0008-1210
- Generic Name
- Desvenlafaxine Succinate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPristiq Extended-release NDC 0008-1211
- Generic Name
- Desvenlafaxine Succinate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPristiq Extended-release NDC 0008-1222
- Generic Name
- Desvenlafaxine Succinate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPremarin NDC 0046-1100
- Generic Name
- Estrogens, Conjugated
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPremarin NDC 0046-1101
- Generic Name
- Estrogens, Conjugated
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPremarin NDC 0046-1102
- Generic Name
- Estrogens, Conjugated
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPremarin NDC 0046-1103
- Generic Name
- Estrogens, Conjugated
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPremarin NDC 0046-1104
- Generic Name
- Estrogens, Conjugated
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPrempro 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 DrugPrempro 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 DrugPrempro 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 DrugPrempro 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 DrugPremphase NDC 0046-2575
- Generic Name
- Conjugated Estrogens And Medroxyprogesterone Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
