NDC Product
Human Prescription DrugArmour Thyroid NDC 50090-0189
- Generic Name
- Thyroid, Porcine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Calcium Stearate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 776XM7047L.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 1592-23-0 and the RxNorm Concept ID (RxCUI) 47633. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
CALCIUM STEARATE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
776XM7047L
The specific atomic composition represented as a molecular structure string.
InChIKey
2C18H35O2.Ca International Chemical Identifier digital signature for unique molecular identification.
SMILES String
CJZGTCYPCWQAJB-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.[Ca+2].C([O-])(=O)CCCCCCCCCCCCCCCCC
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Calcium 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
CALCIUM STEARATE
OF
Common Names & Synonyms
AULABRITE CA 65
CN
BAERLOCHER 5862
CN
CALCII STEARAS [WHO-IP LATIN]
CN
CALCIUM OCTADECANOATE [WHO-IP]
CN
CALCIUM STEARATE [EP MONOGRAPH]
CN
CALCIUM STEARATE [FCC]
CN
CALCIUM STEARATE [HSDB]
CN
CALCIUM STEARATE [II]
CN
CALCIUM STEARATE [JAN]
CN
CALCIUM STEARATE [MART.]
CN
CALCIUM STEARATE [MI]
CN
CALCIUM STEARATE [VANDF]
CN
CALCIUM STEARATE [WHO-DD]
CN
CALCIUM STEARATE [WHO-IP]
CN
E-470(I)STEARIC ACID, CALCIUM SALT
CN
INS NO.470(I)STEARIC ACID, CALCIUM SALT
CN
INS-470(I)STEARIC ACID, CALCIUM SALT
CN
NISSAN CALCIUM STEARATE S
CN
OCTADECANOIC ACID, CALCIUM SALT
CN
STAVINOR CECAVON CA
CN
STEARIC ACID, CALCIUM SALT
CN
Brand / Trade Names
CALSTAR
BN
Systematic Nomenclature
CALCIUM DISTEARATE
SYS
NDC Products Containing CALCIUM 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
A-S Medication Solutions
Active Listing
NDC Product
Human Prescription DrugArmour Thyroid NDC 50090-0190
- Generic Name
- Thyroid, Porcine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugLithium Carbonate NDC 50090-1470
- Generic Name
- Lithium Carbonate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugArmour Thyroid NDC 50090-1692
- Generic Name
- Thyroid, Porcine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 50090-1846
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan NDC 50090-2017
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefuroxime Axetil NDC 50090-2158
- Generic Name
- Cefuroxime Axetil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefuroxime Axetil NDC 50090-2159
- Generic Name
- Cefuroxime Axetil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNitroglycerin NDC 50090-3266
- Generic Name
- Nitroglycerin
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 50090-3646
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNp Thyroid 30 NDC 50090-4376
- Generic Name
- Levothyroxine, Liothyronine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 50090-4906
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNp Thyroid 60 NDC 50090-5216
- Generic Name
- Levothyroxine, Liothyronine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugNp Thyroid 90 NDC 50090-5229
- Generic Name
- Levothyroxine, Liothyronine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 50090-5361
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 50090-5378
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 50090-5379
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 50090-5553
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 50090-5793
- Generic Name
- Pantoprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 50090-5794
- Generic Name
- Pantoprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGemfibrozil NDC 50090-5808
- Generic Name
- Gemfibrozil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLithium Carbonate NDC 50090-6052
- Generic Name
- Lithium Carbonate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 50090-6699
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 50090-6700
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNitroglycerin NDC 50090-6818
- Generic Name
- Nitroglycerin
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydrochlorothiazide NDC 50090-6931
- Generic Name
- Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan NDC 50090-6938
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNitrostat NDC 50090-7203
- Generic Name
- Nitroglycerin
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugGemfibrozil NDC 50090-7233
- Generic Name
- Gemfibrozil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGemfibrozil NDC 50090-7234
- Generic Name
- Gemfibrozil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 50090-7512
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGemfibrozil NDC 50090-7809
- Generic Name
- Gemfibrozil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Acella Pharmaceuticals, LLC
NDC Product
Human Prescription DrugNp Thyroid 15 NDC 42192-327
- Generic Name
- Levothyroxine, Liothyronine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Actavis Pharma, Inc.
NDC Product
Drug For Further Processing- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals
NDC Product
Human Otc DrugJba Goutamin NDC 13411-873
- Generic Name
- Atractylodes Macrocephala ,carica Papaya,curcuma Longa,fibra...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Alembic Pharmaceuticals Limited
NDC Product
Human Prescription DrugLithium Carbonate NDC 46708-148
- Generic Name
- Lithium Carbonate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAripiprazole NDC 46708-260
- Generic Name
- Aripiprazole
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAripiprazole NDC 46708-261
- Generic Name
- Aripiprazole
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
Allergan, Inc.
NDC Product
Human Prescription DrugArmour Thyroid NDC 0456-0457
- Generic Name
- Thyroid, Porcine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugArmour Thyroid NDC 0456-0458
- Generic Name
- Thyroid, Porcine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugArmour Thyroid NDC 0456-0459
- Generic Name
- Thyroid, Porcine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugArmour Thyroid NDC 0456-0460
- Generic Name
- Thyroid, Porcine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugArmour Thyroid NDC 0456-0461
- Generic Name
- Thyroid, Porcine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugArmour Thyroid NDC 0456-0462
- Generic Name
- Thyroid, Porcine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugArmour Thyroid NDC 0456-0463
- Generic Name
- Thyroid, Porcine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugArmour Thyroid NDC 0456-0464
- Generic Name
- Thyroid, Porcine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Amerisource Bergen
NDC Product
Human Otc DrugGood Neighbor Pharmacy Antacid Extra Strength NDC 46122-150
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Aphena Pharma Solutions - Tennessee, LLC
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 43353-978
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvPAK
NDC Product
Human Prescription DrugGemfibrozil NDC 50268-350
- Generic Name
- Gemfibrozil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan NDC 50268-441
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan NDC 50268-442
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 50268-740
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bell Pharmaceuticals, Inc
NDC Product
Human Otc DrugJet Alert Double Strength NDC 15579-200
- Generic Name
- Caffine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugJet Alert Regular Strength NDC 15579-201
- Generic Name
- Caffeine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Burel Pharmaceuticals, LLC
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 35573-428
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
CLINIQUE LABORATORIES LLC
NDC Product
Human Otc DrugEven Better Clinical Acne Solutions NDC 49527-114
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Calvin Scott & Co Inc.
NDC Product
Human Otc DrugNp Thyroid NDC 17224-502
- Generic Name
- Thyroid Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugNp Thyroid NDC 17224-502
- Generic Name
- Thyroid Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugNp Thyroid NDC 17224-502
- Generic Name
- Thyroid Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugNp Thyroid NDC 17224-503
- Generic Name
- Thyroid Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugNp Thyroid NDC 17224-503
- Generic Name
- Thyroid Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugNp Thyroid NDC 17224-503
- Generic Name
- Thyroid Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugNp Thyroid NDC 17224-504
- Generic Name
- Thyroid Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugNp Thyroid NDC 17224-504
- Generic Name
- Thyroid Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugNp Thyroid NDC 17224-504
- Generic Name
- Thyroid Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugNp Thyroid NDC 17224-505
- Generic Name
- Thyroid Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugNp Thyroid NDC 17224-505
- Generic Name
- Thyroid Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugNp Thyroid NDC 17224-505
- Generic Name
- Thyroid Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugNp Thyroid NDC 17224-511
- Generic Name
- Thyroid Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugNp Thyroid NDC 17224-511
- Generic Name
- Thyroid Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugNp Thyroid NDC 17224-511
- Generic Name
- Thyroid Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugGemfibrozil NDC 31722-128
- Generic Name
- Gemfibrozil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 31722-712
- Generic Name
- Pantoprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 31722-713
- Generic Name
- Pantoprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan NDC 31722-729
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan NDC 31722-730
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIrbesartan NDC 31722-731
- Generic Name
- Irbesartan
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Davion, Inc.
NDC Product
Human Otc DrugProtective Powder NDC 42669-233
- Generic Name
- Zinc Oxide
- Dosage Form
- Powder
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Dr. Reddys Laboratories Inc
NDC Product
Human Prescription DrugNitroglycerin NDC 43598-435
- Generic Name
- Nitroglycerin
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNitroglycerin NDC 43598-436
- Generic Name
- Nitroglycerin
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNitroglycerin NDC 43598-437
- Generic Name
- Nitroglycerin
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
ENDO USA, Inc.
NDC Product
Human Prescription DrugSodium Phenylbutyrate NDC 49884-170
- Generic Name
- Sodium Phenylbutyrate Tablets, 500 Mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Edenbridge Pharmaceuticals LLC.
NDC Product
Human Prescription DrugEthacrynic Acid NDC 42799-405
- Generic Name
- Ethacrynic Acid
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Endo USA, Inc.
NDC Product
Human Prescription DrugPimozide NDC 49884-347
- Generic Name
- Pimozide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPimozide NDC 49884-348
- Generic Name
- Pimozide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAliskiren NDC 49884-424
- Generic Name
- Aliskiren
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAliskiren NDC 49884-425
- Generic Name
- Aliskiren
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
HEB
NDC Product
Human Otc DrugHeb Extra Strength Original Flavor NDC 37808-505
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugHeb Extra Strength Cherry Flavor NDC 37808-510
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugTums Ex NDC 0135-0076
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGaviscon Extra Strength NDC 0135-0098
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Ex NDC 0135-0140
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Ex NDC 0135-0154
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Extra Strength Sugar-free NDC 0135-0155
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Smoothies NDC 0135-0227
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGaviscon Extra Strength NDC 0135-0430
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Ex NDC 0135-0521
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Naturals NDC 0135-1326
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Naturals NDC 0135-1328
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAdvil Pm NDC 0573-0164
- Generic Name
- Diphenhydramine Citrate And Ibuprofen
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Have & Be Co., Ltd.
NDC Product
Human Otc DrugDr.jart Cicapair Tiger Grass Color Correcting Treatment NDC 49404-147
- Generic Name
- Zinc Oxide, Titanium Dioxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDr.jart Cicapair Tiger Grass Camo Drops NDC 49404-152
- Generic Name
- Zinc Oxide, Titanium Dioxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
NDC Product
Human Prescription DrugLithium Carbonate NDC 23155-763
- Generic Name
- Lithium Carbonate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugLithium Carbonate NDC 0054-0021
- Generic Name
- Lithium Carbonate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLithium Carbonate NDC 0054-2526
- Generic Name
- Lithium Carbonate
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLithium Carbonate NDC 0054-2527
- Generic Name
- Lithium Carbonate
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLithium Carbonate NDC 0054-2531
- Generic Name
- Lithium Carbonate
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLithium Carbonate NDC 0054-4527
- Generic Name
- Lithium Carbonate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLithium Carbonate NDC 0054-8526
- Generic Name
- Lithium Carbonate
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLithium Carbonate NDC 0054-8527
- Generic Name
- Lithium Carbonate
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLithium Carbonate NDC 0054-8528
- Generic Name
- Lithium Carbonate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Indoco Remedies Limited
NDC Product
Human Prescription DrugLofexidine NDC 14445-146
- Generic Name
- Lofexidine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Ingenus Pharmaceuticals, LLC
NDC Product
Human Prescription DrugHemiclor NDC 50742-285
- Generic Name
- Chlorthalidone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Lil Drug Store Products, Inc
NDC Product
Human Otc Drug- Generic Name
- Advil Pm
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
MEIJER DISTRIBUTION INC
NDC Product
Human Otc DrugMeijer Extra Strength Original Flavor NDC 41250-675
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Macleods Pharmaceuticals Limited
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 33342-159
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Major Pharmaceuticals
NDC Product
Human Otc DrugAcid Gone Antacid Extra Strength NDC 0904-5365
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 0904-6474
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHaloperidol NDC 0904-6661
- Generic Name
- Haloperidol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 0904-6870
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 0904-7383
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefuroxime Axetil NDC 0904-7542
- Generic Name
- Cefuroxime Axetil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugFerric Citrate NDC 0378-2895
- Generic Name
- Ferric Citrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 0378-6688
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 0378-6689
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 0615-7629
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 0615-8055
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 0615-8113
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGemfibrozil NDC 0615-8354
- Generic Name
- Gemfibrozil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
PD-Rx Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugCefuroxime Axetil NDC 43063-656
- Generic Name
- Cefuroxime Axetil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefuroxime Axetil NDC 43063-657
- Generic Name
- Cefuroxime Axetil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 43063-725
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGemfibrozil NDC 43063-745
- Generic Name
- Gemfibrozil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 43063-947
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Par Health USA, LLC
NDC Product
Human Prescription DrugSodium Phenylbutyrate NDC 49884-006
- Generic Name
- Sodium Phenylbutyrate
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- ANDA
Active Listing
Parke-Davis Div of Pfizer Inc
NDC Product
Human Prescription DrugLopid NDC 0071-0737
- Generic Name
- Gemfibrozil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Pharmacia & Upjohn Company LLC
NDC Product
Human Prescription DrugCortef NDC 0009-0012
- Generic Name
- Hydrocortisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMedrol NDC 0009-0020
- Generic Name
- Methylprednisolone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMedrol NDC 0009-0022
- Generic Name
- Methylprednisolone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCortef NDC 0009-0031
- Generic Name
- Hydrocortisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCortef NDC 0009-0044
- Generic Name
- Hydrocortisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMedrol NDC 0009-0056
- Generic Name
- Methylprednisolone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMedrol NDC 0009-0073
- Generic Name
- Methylprednisolone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
QPharma Inc
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 42708-104
- Generic Name
- Pantoprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 42708-180
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 42708-185
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
RITE AID CORPORATION
NDC Product
Human Otc DrugRite Aid Extra Strength NDC 11822-1050
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRite Aid Extra Strength NDC 11822-1051
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rising Pharma Holdings, Inc.
NDC Product
Human Prescription DrugGemfibrozil NDC 16571-784
- Generic Name
- Gemfibrozil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Safecor Health LLC
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 48433-081
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sandoz Inc
NDC Product
Human Prescription DrugGriseofulvin NDC 0781-5514
- Generic Name
- Griseofulvin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGriseofulvin NDC 0781-5515
- Generic Name
- Griseofulvin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugUltramicrosize Griseofulvin NDC 0781-5827
- Generic Name
- Ultramicrosize Griseofulvin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugUltramicrosize Griseofulvin NDC 0781-5828
- Generic Name
- Ultramicrosize Griseofulvin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
ScieGen Pharmaceuticals Inc
NDC Product
Human Prescription DrugEthacrynic Acid NDC 50228-334
- Generic Name
- Ethacrynic Acid
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sigmapharm Laboratories, LLC
NDC Product
Human Prescription DrugSodium Phenylbutyrate NDC 42794-086
- Generic Name
- Sodium Phenylbutyrate
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- ANDA
Active Listing
Solco Healthcare U.S., LLC
NDC Product
Human Prescription DrugNitroglycerin NDC 43547-985
- Generic Name
- Nitroglycerin
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNitroglycerin NDC 43547-986
- Generic Name
- Nitroglycerin
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNitroglycerin NDC 43547-987
- Generic Name
- Nitroglycerin
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
Sunrise Pharmaceutical, Inc.
NDC Product
Human Prescription DrugDiazepam NDC 11534-199
- Generic Name
- Diazepam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiazepam NDC 11534-202
- Generic Name
- Diazepam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiazepam NDC 11534-203
- Generic Name
- Diazepam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
TARGET CORPORATION
NDC Product
Human Otc DrugExtra Strength Antacid NDC 11673-814
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
THE KROGER CO.,
NDC Product
Human Otc DrugKroger Extra Strength NDC 30142-610
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Tarte, Inc.
NDC Product
Human Otc DrugFoundcealer Multi-tasking Foundation Broad Spectrum Spf 20 Sunscreen 8b Porcelain Beige NDC 51060-197
- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFoundcealer Multi-tasking Foundation Broad Spectrum Spf 20 Sunscreen 16b Fair-light Beige NDC 51060-200
- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFoundcealer Multi-tasking Foundation Broad Spectrum Spf 20 Sunscreen 16s Fair-light Sand NDC 51060-201
- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFoundcealer Multi-tasking Foundation Broad Spectrum Spf 20 Sunscreen 16n Fair-light Neutral NDC 51060-202
- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFoundcealer Multi-tasking Foundation Broad Spectrum Spf 20 Sunscreen 22n Light Neutral NDC 51060-204
- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFoundcealer Multi-tasking Foundation Broad Spectrum Spf 20 Sunscreen 27s Light-medium Sand NDC 51060-207
- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFoundcealer Multi-tasking Foundation Broad Spectrum Spf 20 Sunscreen 27n Light-medium Neutral NDC 51060-208
- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFoundcealer Multi-tasking Foundation Broad Spectrum Spf 20 Sunscreen 29h Light-medium Honey NDC 51060-209
- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFoundcealer Multi-tasking Foundation Broad Spectrum Spf 20 Sunscreen 34n Medium Neutral NDC 51060-211
- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFoundcealer Multi-tasking Foundation Broad Spectrum Spf 20 Sunscreen 35g Medium Golden NDC 51060-212
- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFoundcealer Multi-tasking Foundation Broad Spectrum Spf 20 Sunscreen 36h Medium-tan Honey NDC 51060-213
- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFoundcealer Multi-tasking Foundation Broad Spectrum Spf 20 Sunscreen 36n Medium-tan Neutral NDC 51060-214
- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFoundcealer Multi-tasking Foundation Broad Spectrum Spf 20 Sunscreen 38s Medium-tan Sand NDC 51060-215
- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Titanium Dioxide And Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugNeomycin Sulfate NDC 0093-1177
- Generic Name
- Neomycin Sulfate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugJinteli NDC 0093-3122
- Generic Name
- Norethindrone Acetate And Ethinyl Estradiol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTri-legest Fe 28 Day NDC 0555-9032
- Generic Name
- Norethindrone Acetate And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 50111-456
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugFerric Citrate NDC 0480-2996
- Generic Name
- Ferric Citrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Torrent Pharmaceuticals Limited
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 13668-096
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 13668-429
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREEN CO.
NDC Product
Human Otc DrugFast Acting Heartburn Relief NDC 0363-1155
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Wal-Mart Stores,Inc
NDC Product
Human Otc DrugEquate Extra Strength Antacid NDC 49035-105
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
NDC Product
Human Prescription DrugProtonix Delayed-release NDC 0008-0841
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugProtonix Delayed-release NDC 0008-0843
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugProtonix Delayed-release NDC 0008-0844
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
sanofi-aventis U.S. LLC
NDC Product
Human Prescription DrugPriftin NDC 0088-2102
- Generic Name
- Rifapentine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
