NDC Product
Human Prescription DrugFelodipine NDC 50090-1124
- Generic Name
- Felodipine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Magnesium Oxide, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 3A3U0GI71G.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 1309-48-4 and the RxNorm Concept ID (RxCUI) 6582. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
MAGNESIUM OXIDE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
3A3U0GI71G
The specific atomic composition represented as a molecular structure string.
InChIKey
Mg.O International Chemical Identifier digital signature for unique molecular identification.
SMILES String
AXZKOIWUVFPNLO-UHFFFAOYSA-N 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
[O-2].[Mg+2]
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Magnesium Oxide. 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 OXIDE
OF
Common Names & Synonyms
HEAVY MAGNESIUM OXIDE
CN
LIGHT MAGNESIUM OXIDE [WHO-IP]
CN
MAGNESIA [VANDF]
CN
MAGNESIA OXYDATA
CN
MAGNESIA OXYDATA [HPUS]
CN
MAGNESII OXIDUM [WHO-IP LATIN]
CN
MAGNESIUM (AS OXIDE) [VANDF]
CN
MAGNESIUM OXIDE [FCC]
CN
MAGNESIUM OXIDE [HSDB]
CN
MAGNESIUM OXIDE [II]
CN
MAGNESIUM OXIDE [JAN]
CN
MAGNESIUM OXIDE [MART.]
CN
MAGNESIUM OXIDE [MI]
CN
MAGNESIUM OXIDE [ORANGE BOOK]
CN
MAGNESIUM OXIDE [USP MONOGRAPH]
CN
MAGNESIUM OXIDE [USP-RS]
CN
MAGNESIUM OXIDE [VANDF]
CN
MAGNESIUM OXIDE [WHO-DD]
CN
MAGNESIUM OXIDE [WHO-IP]
CN
MAGNESIUM OXIDE HEAVY [WHO-DD]
CN
MAGNESIUM OXIDE, HEAVY
CN
MAGNESIUM OXIDE, HEAVY [EP IMPURITY]
CN
MAGNESIUM OXIDE, HEAVY [EP MONOGRAPH]
CN
MAGNESIUM OXIDE, LIGHT
CN
MAGNESIUM OXIDE, LIGHT [EP MONOGRAPH]
CN
MAGNESIUM OXIDE, LIGHT [II]
CN
Brand / Trade Names
CLENPIQ COMPONENT MAGNESIUM OXIDE
BN
Technical Codes
E-530
CD
INS NO.530
CD
INS-530
CD
NDC Products Containing MAGNESIUM OXIDE
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
A-S Medication Solutions
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Mint Flavor NDC 50090-3560
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRabeprazole Sodium NDC 50090-4751
- Generic Name
- Rabeprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin Calcium NDC 50090-5188
- Generic Name
- Rosuvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin Calcium NDC 50090-5189
- Generic Name
- Rosuvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin Calcium NDC 50090-5468
- Generic Name
- Rosuvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6087
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6089
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6090
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6100
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6101
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6103
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6104
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6105
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6115
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6116
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6118
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6119
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin Calcium NDC 50090-6422
- Generic Name
- Rosuvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6579
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6602
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6610
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6634
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6660
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRabeprazole Sodium NDC 50090-6887
- Generic Name
- Rabeprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 50090-6919
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
APNAR PHARMA LP
NDC Product
Human Otc DrugMagnesium Oxide NDC 24689-132
- Generic Name
- Magnesium Oxide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
ATLANTIC BIOLOGICALS CORP.
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Mint Flavor NDC 17856-1362
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
Accord Healthcare Inc.
NDC Product
Human Prescription DrugPravastatin Sodium NDC 16729-008
- Generic Name
- Pravastatin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPravastatin Sodium NDC 16729-009
- Generic Name
- Pravastatin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPravastatin Sodium NDC 16729-010
- Generic Name
- Pravastatin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPravastatin Sodium NDC 16729-011
- Generic Name
- Pravastatin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin NDC 16729-284
- Generic Name
- Rosuvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin NDC 16729-285
- Generic Name
- Rosuvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin NDC 16729-286
- Generic Name
- Rosuvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin NDC 16729-287
- Generic Name
- Rosuvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 16729-447
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 16729-448
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 16729-449
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 16729-450
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 16729-451
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 16729-452
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 16729-453
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 16729-454
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 16729-455
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 16729-456
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 16729-457
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 16729-458
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Acella Pharmaceuticals, LLC
NDC Product
Human Prescription DrugPnv-select NDC 42192-320
- Generic Name
- Vitamin A Acetate, Ascorbic Acid, Cholecalciferol, Alpha-toc...
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugPnv-omega NDC 42192-332
- Generic Name
- Ascorbic Acid, Cholecalciferol, .alpha.-tocopherol, Pyridoxi...
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions
NDC Product
Human Otc DrugTerrasil Infection Protection Wound Care NDC 24909-030
- Generic Name
- Allantoin
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Allantoin
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Skin Repair NDC 24909-032
- Generic Name
- Allantoin
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Diabetics Ulcer And Sore Relief NDC 24909-034
- Generic Name
- Allantoin
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Bed Sore And Pressure Sore Relief NDC 24909-035
- Generic Name
- Allantoin
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Tinea Antifungal Cleansing Bar NDC 24909-036
- Generic Name
- Thuja Occidentalis Whole
- Dosage Form
- Soap
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugTerrasil Antifungal Cleansing Bar NDC 24909-037
- Generic Name
- Clotrimazole
- Dosage Form
- Soap
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil The Fungal Solution Kit NDC 24909-038
- Generic Name
- Clotrimazole
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Diabetics Ulcer And Sore Relief Kit NDC 24909-039
- Generic Name
- Allantoin
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil First Aid Antiseptic Wound And Burn Care Kit NDC 24909-040
- Generic Name
- Hexylresorcinol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil First Aid Antiseptic Wound And Burn Care NDC 24909-041
- Generic Name
- Hexylresorcinol
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Eczema And Psoriasis Severe Outbreak NDC 24909-060
- Generic Name
- Graphite, Sodium Chloride, Symphytum Officinale Whole, Thuja...
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugTerragen Hg Formula Maximum Strength NDC 24909-062
- Generic Name
- Graphite, Sodium Chloride, Symphytum Officinale Whole, Thuja...
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Aidance Scientific, Inc.
NDC Product
Human Otc DrugFemmesil Ultra Therapy NDC 24909-050
- Generic Name
- Clotrimazole
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Fast And Natural Wart Removal NDC 24909-051
- Generic Name
- Graphite 10x, Natrum Muriaticum 3x, Symphytum Officinale (co...
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions
NDC Product
Human Otc DrugTerrasil Scar Recovery NDC 24909-043
- Generic Name
- Allantoin
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Foot Ulcer And Sore Relief NDC 24909-044
- Generic Name
- Allantoin
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Jock Itch Antifungal Cleansing Bar NDC 24909-045
- Generic Name
- Thuja Occidentalis
- Dosage Form
- Soap
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugTerrasil Fungal Treatment NDC 24909-046
- Generic Name
- Clotrimazole
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Diabetics Ulcer And Bed Sore Relief NDC 24909-048
- Generic Name
- Allantoin
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil First Aid Antiseptic Wound And Burn Care NDC 24909-049
- Generic Name
- Hexylresorcinol
- Dosage Form
- Kit
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Ringworm Treatment Max NDC 24909-102
- Generic Name
- Clotrimazole
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Tinea Treatment Max NDC 24909-104
- Generic Name
- Clotrimazole
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Anti-fungal Treatment Max NDC 24909-106
- Generic Name
- Clotrimazole
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Balanitis Relief NDC 24909-119
- Generic Name
- Sulfur, Symphytum Officinale (comfrey)
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugTerrasil Athletes Foot Antifungal Treatment Max NDC 24909-207
- Generic Name
- Clotrimazole
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Jockitch Treatment Maximum Strength NDC 24909-212
- Generic Name
- Clotrimazole
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Aidance Skincare & Topical Solutions, LLC
NDC Product
Human Otc DrugTerrasil Ringworm Anti-fungal Cleansing Bar 75g NDC 24909-204
- Generic Name
- Thuja Occidentalis 6x Hpus
- Dosage Form
- Soap
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugTterrasil Athletes Foot Cleansing Bar NDC 24909-210
- Generic Name
- Thuja Occidentalis
- Dosage Form
- Soap
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugFemmesil Cleansing Bar NDC 24909-211
- Generic Name
- Thuja Occidentalis
- Dosage Form
- Soap
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugTerrasil Jock Itch Treatment Maximum Strength NDC 24909-214
- Generic Name
- Clotrimazole
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTerrasil Antifungal Cleansing Bar NDC 24909-217
- Generic Name
- Thuja Occidentalis
- Dosage Form
- Soap
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Ajanta Pharma USA Inc.
NDC Product
Human Prescription DrugNaproxen And Esomeprazole Magnesium NDC 27241-202
- Generic Name
- Naproxen And Esomeprazole Magnesium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNaproxen And Esomeprazole Magnesium NDC 27241-203
- Generic Name
- Naproxen And Esomeprazole Magnesium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Albertsons Companies
NDC Product
Human Otc DrugOmeprazole Magnesium NDC 21130-398
- Generic Name
- Omeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Allegis Pharmaceuticals, LLC
NDC Product
Human Otc DrugMag 440 NDC 28595-710
- Generic Name
- Megnesium Oxide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Amerisource Bergen
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 46122-736
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 46122-821
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
AmerisourceBergen (Good Neighbor Pharmacy) 46122
NDC Product
Human Otc DrugNicotine Polacrilex Coated Ice Mint NDC 46122-448
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Polacrilex Coated Ice Mint NDC 46122-449
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Polacrilex NDC 46122-717
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Polacrilex NDC 46122-718
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Polacrilex NDC 46122-720
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 46122-724
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Polacrilex NDC 46122-725
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aurolife Pharma LLC
NDC Product
Human Prescription DrugClorazepate Dipotassium NDC 13107-282
- Generic Name
- Clorazepate Dipotassium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClorazepate Dipotassium NDC 13107-283
- Generic Name
- Clorazepate Dipotassium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClorazepate Dipotassium NDC 13107-284
- Generic Name
- Clorazepate Dipotassium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvKARE
NDC Product
Human Prescription DrugPitavastatin NDC 42291-905
- Generic Name
- Pitavastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPitavastatin NDC 42291-906
- Generic Name
- Pitavastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPitavastatin NDC 42291-907
- Generic Name
- Pitavastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Better Living Brands LLC
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 21130-100
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
CarWin Pharmaceutical Associates, LLC
NDC Product
Human Prescription DrugQuflora Pediatric NDC 15370-103
- Generic Name
- Vitamin A Acetate, Ascorbic Acid, Cholecalciferol, .alpha.-t...
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugQuflora Pediatric NDC 15370-104
- Generic Name
- Vitamin A Acetate, Ascorbic Acid, Cholecalciferol, .alpha.-t...
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugQuflora Pediatric NDC 15370-105
- Generic Name
- Vitamin A Acetate, Ascorbic Acid, Cholecalciferol, .alpha.-t...
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugTristart Dha NDC 15370-250
- Generic Name
- Ascorbic Acid, Cholecalciferol, .alpha.-tocopherol Acetate, ...
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Chiesi USA, Inc.
NDC Product
Human Prescription DrugFerriprox NDC 10122-104
- Generic Name
- Deferiprone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Deseret Biologicals, Inc.
NDC Product
Human Otc DrugConnection NDC 43742-2544
- Generic Name
- Anacardium Orientale, Aurum Muriaticum Natronatum, Camphora,...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Dr. Reddy's Laboratories Inc
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 43598-407
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Dr. Reddy's Laboratories Inc.
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 43598-812
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugOmeprazole Magnesium NDC 43598-813
- Generic Name
- Omeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Endo USA
NDC Product
Human Otc DrugMagnesium Oxide NDC 0603-0209
- Generic Name
- Magnesium Oxide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMagnesium Oxide NDC 0603-0213
- Generic Name
- Magnesium Oxide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Exeltis USA, Inc.
NDC Product
Human Prescription DrugVitafol One NDC 0642-0070
- Generic Name
- Prenatal Supplement With Dha
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugSelect-ob Plus Dha Prenatal Supplement Plus Dha NDC 0642-0075
- Generic Name
- .beta.-carotene, Vitamin A Acetate, Ascorbic Acid, Cholecalc...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugVitafol Ultra NDC 0642-0093
- Generic Name
- Doconexent, Niacinamide, .alpha.-tocopherol Acetate, Dl-, Ch...
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugStrovite One Caplets NDC 0642-0207
- Generic Name
- Vitamin A, Calcium Pantothenate, Ascorbic Acid, Cholecalcife...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugVitafol Fe Plus NDC 0642-7473
- Generic Name
- Doconexent, Niacinamide, .alpha.-tocopherol Acetate, Dl-, Ch...
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Genomma Lab USA
NDC Product
Human Otc DrugBufferin Regular Strength Pain Relief NDC 50066-610
- Generic Name
- Aspirin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
HEB
NDC Product
Human Otc DrugOmeprazole Magnesium NDC 37808-006
- Generic Name
- Omeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 37808-115
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hahnemann Laboratories, INC.
NDC Product
Human Otc DrugMagnesia Oxydata NDC 37662-0965
- Generic Name
- Magnesia Oxydata
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugMagnesia Oxydata NDC 37662-0966
- Generic Name
- Magnesia Oxydata
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugMagnesia Oxydata NDC 37662-0967
- Generic Name
- Magnesia Oxydata
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugMagnesia Oxydata NDC 37662-0968
- Generic Name
- Magnesia Oxydata
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugMagnesia Oxydata NDC 37662-0969
- Generic Name
- Magnesia Oxydata
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugMagnesia Oxydata NDC 37662-0970
- Generic Name
- Magnesia Oxydata
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugMagnesia Oxydata NDC 37662-0971
- Generic Name
- Magnesia Oxydata
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugMagnesia Oxydata NDC 37662-0972
- Generic Name
- Magnesia Oxydata
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugNicorette Original NDC 0135-0157
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Original NDC 0135-0158
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Mint NDC 0135-0229
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Mint NDC 0135-0230
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Fruit Chill NDC 0135-0241
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Fruit Chill NDC 0135-0242
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Spearmint Burst NDC 0135-0355
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Cinnamon Surge NDC 0135-0466
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Cinnamon Surge NDC 0135-0467
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette White Ice Mint NDC 0135-0474
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette White Ice Mint NDC 0135-0475
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Spearmint Burst NDC 0135-0532
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Spearmint Burst NDC 0135-0533
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
Lil' Drug Store Products, Inc.
NDC Product
Human Otc DrugNicorette Fruit Chill Nicotine Polacrilex NDC 29485-5270
- Generic Name
- Nicotine
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette White Mint Nicotine Polacrilex NDC 29485-5271
- Generic Name
- Nicotine
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
Macleods Pharmaceuticals Limited
NDC Product
Human Prescription DrugTelmisartan NDC 33342-118
- Generic Name
- Telmisartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTelmisartan NDC 33342-119
- Generic Name
- Telmisartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTelmisartan NDC 33342-120
- Generic Name
- Telmisartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Marlex Pharmaceuticals Inc
NDC Product
Human Otc DrugMagnesium Oxide NDC 10135-786
- Generic Name
- Magnesium Oxide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Marlex Pharmaceuticals Inc.
NDC Product
Human Otc DrugMagnesium Oxide NDC 10135-721
- Generic Name
- Magnesium Oxide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugPhenytek NDC 0378-2670
- Generic Name
- Extended Phenytoin Sodium
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhenytek NDC 0378-3750
- Generic Name
- Phenytoin Sodium
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPitavastatin Calcium NDC 0378-5055
- Generic Name
- Pitavastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPitavastatin Calcium NDC 0378-5056
- Generic Name
- Pitavastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPitavastatin Calcium NDC 0378-5057
- Generic Name
- Pitavastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugExtended Phenytoin Sodium NDC 0615-8556
- Generic Name
- Phenytoin Sodium
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEsomeprazole Magnesium NDC 0615-8628
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
PD-Rx Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugPravastatin Sodium NDC 43063-807
- Generic Name
- Pravastatin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPravastatin Sodium NDC 43063-808
- Generic Name
- Pravastatin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
QPharma Inc
NDC Product
Human Prescription DrugOmeprazole NDC 42708-170
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rugby Laboratories
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Mint Flavor NDC 0536-1362
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Mint Flavor NDC 0536-1372
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Coated Mint Flavor NDC 0536-3112
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Coated Mint Flavor NDC 0536-3113
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Coated Fruit Flavor NDC 0536-3386
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Coated Fruit Flavor NDC 0536-3387
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
Sandoz Inc
NDC Product
Human Prescription DrugOmeprazole NDC 0781-2785
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 0781-2790
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 0781-2859
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 0781-2868
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sun Pharmaceutical Industries, Inc.
NDC Product
Human Otc DrugCetirizine Hydrochloride NDC 47335-343
- Generic Name
- Cetirizine Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugCetirizine Hydrochloride NDC 47335-344
- Generic Name
- Cetirizine Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEzallor Sprinkle NDC 47335-984
- Generic Name
- Rosuvastatin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugEzallor Sprinkle NDC 47335-985
- Generic Name
- Rosuvastatin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugEzallor Sprinkle NDC 47335-986
- Generic Name
- Rosuvastatin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugEzallor Sprinkle NDC 47335-987
- Generic Name
- Rosuvastatin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugAmiloride Hydrochloride And Hydrochlorothiazide NDC 0555-0483
- Generic Name
- Amiloride Hydrochloride And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugPitavastatin NDC 0480-3631
- Generic Name
- Pitavastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPitavastatin NDC 0480-3632
- Generic Name
- Pitavastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPitavastatin NDC 0480-3633
- Generic Name
- Pitavastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
The Kroger Co.
NDC Product
Human Otc DrugOmeprazole Magnesium NDC 30142-012
- Generic Name
- Omeprazole Magnesium 20.6mg Capsules
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 30142-261
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Torrent Pharmaceuticals Limited
NDC Product
Human Prescription DrugRabeprazole Sodium NDC 13668-107
- Generic Name
- Rabeprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFelodipine NDC 13668-132
- Generic Name
- Felodipine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFelodipine NDC 13668-133
- Generic Name
- Felodipine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFelodipine NDC 13668-134
- Generic Name
- Felodipine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREEN CO.
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 0363-0361
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 0363-0508
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Wal-Mart Stores Inc
NDC Product
Human Otc DrugOmeprazole Magnesium NDC 49035-397
- Generic Name
- Omeprazole Magnesium 20.6mg Capsules
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Wal-Mart Stores, Inc.
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 49035-980
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreens
NDC Product
Human Otc DrugNicotine Polacrilex Mint NDC 0363-1420
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Polacrilex Mint NDC 0363-1421
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
Walgreens Company
NDC Product
Human Otc DrugOmeprazole Magnesium NDC 0363-0042
- Generic Name
- Omeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 0363-3298
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
