NDC Product
Human Prescription DrugOriahnn NDC 0074-1017
- Generic Name
- Elagolix And Estradiol And Norethisterone
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Butyl Alcohol, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 8PJ61P6TS3.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 71-36-3 and the RxNorm Concept ID (RxCUI) 1310579. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
BUTYL ALCOHOL
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
8PJ61P6TS3
The specific atomic composition represented as a molecular structure string.
InChIKey
C4H10O International Chemical Identifier digital signature for unique molecular identification.
SMILES String
LRHPLDYGYMQRHN-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
OCCCC
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Butyl Alcohol. 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
N-BUTYL ALCOHOL
OF
Common Names & Synonyms
1-BUTANOL [USP-RS]
CN
ALCOHOL,BUTYL
CN
ALCOHOL,BUTYL [VANDF]
CN
BUTYL ALCOHOL [FCC]
CN
BUTYL ALCOHOL [FHFI]
CN
BUTYL ALCOHOL [HSDB]
CN
BUTYL ALCOHOL [II]
CN
BUTYL ALCOHOL [MART.]
CN
N-BUTANOL
CN
N-BUTYL ALCOHOL [MI]
CN
N-BUTYL ALCOHOL [WHO-DD]
CN
TRIBUTYL ACETYLCITRATE IMPURITY D [EP IMPURITY]
CN
Systematic Nomenclature
1-BUTANOL
SYS
ALCOHOL, BUTYL
SYS
BUTAN-1-OL
SYS
BUTYL ALCOHOL
SYS
METHYLOLPROPANE
SYS
PROPYLCARBINOL
SYS
Technical Codes
FEMA NO. 2178
CD
NSC-62782
CD
NDC Products Containing BUTYL ALCOHOL
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
AbbVie Inc.
Active Listing
Actavis Pharma, Inc.
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0228-3090
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0228-3091
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0228-3092
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0228-3093
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0228-3116
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0228-3117
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Tetracycline Hydrochloride
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugTetracycline Hydrochloride NDC 0591-2474
- Generic Name
- Tetracycline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTetracycline Hydrochloride NDC 0591-2475
- Generic Name
- Tetracycline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
AiPing Pharmaceutical, Inc.
NDC Product
Human Prescription DrugCelecoxib NDC 11788-112
- Generic Name
- Celecoxib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCelecoxib NDC 11788-113
- Generic Name
- Celecoxib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCelecoxib NDC 11788-114
- Generic Name
- Celecoxib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCelecoxib NDC 11788-115
- Generic Name
- Celecoxib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Amneal Pharmaceuticals of New York LLC
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1277
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1278
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1279
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1280
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1281
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1282
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibric Acid NDC 0115-1324
- Generic Name
- Fenofibric Acid
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibric Acid NDC 0115-1325
- Generic Name
- Fenofibric Acid
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1479
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
AstraZeneca Pharmaceuticals LP
NDC Product
Human Prescription DrugNexium NDC 0186-4010
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-4020
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-4025
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-4040
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-4050
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-5020
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-5040
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugKoselugo NDC 0310-0610
- Generic Name
- Selumetinib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugKoselugo NDC 0310-0625
- Generic Name
- Selumetinib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Aurolife Pharma, LLC
NDC Product
Human Prescription DrugButalbital, Acetaminophen And Caffeine NDC 13107-075
- Generic Name
- Butalbital, Acetaminophen And Caffeine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhentermine NDC 13107-105
- Generic Name
- Phentermine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhentermine NDC 13107-106
- Generic Name
- Phentermine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
E.R. Squibb & Sons, L.L.C.
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
Haleon US Holdings LLC
NDC Product
Human Otc DrugGas-x Total Relief Maximum Strength NDC 0067-0118
- Generic Name
- Calcium Carbonate, Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGas-x Total Relief Maximum Strength NDC 0067-0119
- Generic Name
- Calcium Carbonate, Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites NDC 0135-0183
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Berry Shake NDC 0135-0184
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites NDC 0135-0606
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites NDC 0135-0618
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Peppermint NDC 0135-0623
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites With Gas Relief NDC 0135-0624
- Generic Name
- Calcium Carbonate And Simethicone
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Mixed Fruit NDC 0135-0641
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTums Chewy Bites Orange And Cream Es NDC 0135-0642
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Hikma Pharmaceuticals USA Inc.
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 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 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 DrugCyclophosphamide NDC 0054-0382
- Generic Name
- Cyclophosphamide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCyclophosphamide NDC 0054-0383
- Generic Name
- Cyclophosphamide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugDoxycycline Hyclate NDC 0143-9803
- Generic Name
- Doxycycline Hyclate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Indoco Remedies Limited
NDC Product
Human Prescription DrugPregabalin NDC 14445-123
- Generic Name
- Pregabalin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPregabalin NDC 14445-124
- Generic Name
- Pregabalin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPregabalin NDC 14445-125
- Generic Name
- Pregabalin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPregabalin NDC 14445-126
- Generic Name
- Pregabalin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPregabalin NDC 14445-127
- Generic Name
- Pregabalin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPregabalin NDC 14445-128
- Generic Name
- Pregabalin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPregabalin NDC 14445-173
- Generic Name
- Pregabalin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPregabalin NDC 14445-174
- Generic Name
- Pregabalin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lannett Company Inc.
NDC Product
Human Prescription DrugBupropion Hydrochloride (xl) NDC 0527-2415
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride (xl) NDC 0527-2430
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lannett Company, Inc.
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 0527-0586
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugUrsodiol NDC 0527-1326
- Generic Name
- Ursodiol
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDanazol NDC 0527-1368
- Generic Name
- Danazol
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDanazol NDC 0527-1369
- Generic Name
- Danazol
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDanazol NDC 0527-1392
- Generic Name
- Danazol
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLoxapine NDC 0527-1394
- Generic Name
- Loxapine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLoxapine NDC 0527-1395
- Generic Name
- Loxapine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLoxapine NDC 0527-1396
- Generic Name
- Loxapine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLoxapine NDC 0527-1397
- Generic Name
- Loxapine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugButalbital, Aspirin, And Caffeine NDC 0527-1552
- Generic Name
- Butalbital, Aspirin, And Caffeine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugButalbital, Acetaminophen And Caffeine NDC 0527-4094
- Generic Name
- Butalbital, Acetaminophen And Caffeine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugButalbital, Acetaminophen, And Caffeine NDC 0527-4095
- Generic Name
- Butalbital, Acetaminophen, And Caffeine Capsules
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrazosin NDC 0527-4180
- Generic Name
- Prazosin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrazosin NDC 0527-4181
- Generic Name
- Prazosin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrazosin NDC 0527-4182
- Generic Name
- Prazosin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Major Pharmaceuticals
NDC Product
Human Prescription DrugZiprasidone NDC 0904-6269
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZiprasidone NDC 0904-6270
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZiprasidone NDC 0904-6271
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZiprasidone NDC 0904-6272
- Generic Name
- Ziprasidone
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTemazepam NDC 0904-6436
- Generic Name
- Temazepam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEsomeprazole Magnesium NDC 0904-6581
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMesalamine NDC 0904-6832
- Generic Name
- Mesalamine
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 0904-6860
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 0904-6861
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- 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 DrugAtomoxetine NDC 0904-6908
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPaliperidone NDC 0904-6935
- Generic Name
- Paliperidone
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPaliperidone NDC 0904-6936
- Generic Name
- Paliperidone
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPaliperidone NDC 0904-6937
- Generic Name
- Paliperidone
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 0904-6987
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 0904-6988
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmantadine Hydrochloride NDC 0904-7042
- Generic Name
- Amantadine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTrospium Chloride NDC 0904-7059
- Generic Name
- Trospium Chloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 0904-7182
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSevelamer Hydrochloride NDC 0904-7209
- Generic Name
- Sevelamer Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Parenteral
- 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 DrugMycophenolate Mofetil NDC 0904-7466
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDofetilide NDC 0904-7522
- Generic Name
- Dofetilide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDofetilide NDC 0904-7523
- Generic Name
- Dofetilide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDofetilide NDC 0904-7524
- Generic Name
- Dofetilide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGabapentin NDC 0904-7613
- Generic Name
- Gabapentin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGabapentin NDC 0904-7614
- Generic Name
- Gabapentin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGabapentin NDC 0904-7615
- Generic Name
- Gabapentin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Marlex Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugSelegiline Hydrochloride NDC 10135-737
- Generic Name
- Selegiline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRifabutin NDC 10135-738
- Generic Name
- Rifabutin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugTemodar NDC 0085-1366
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1381
- Generic Name
- Temozolomide
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1417
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1425
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1430
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-1519
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemodar NDC 0085-3004
- Generic Name
- Temozolomide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugBromocriptine Mesylate NDC 0378-7096
- Generic Name
- Bromocriptine Mesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
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 DrugAmantadine Hydrochloride NDC 0615-8263
- Generic Name
- Amantadine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHydrochlorothiazide NDC 0615-8344
- Generic Name
- Hydrochlorothiazide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 0615-8586
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 0615-8587
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 0615-8588
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- 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
Northstar Rx LLC
NDC Product
Human Prescription DrugCarbamazepine NDC 16714-063
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbamazepine NDC 16714-064
- Generic Name
- Carbamazepine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Par Pharmaceutical Inc.
NDC Product
Human Prescription DrugOmega-3-acid Ethyl Esters NDC 0254-3010
- Generic Name
- Omega-3-acid Ethyl Esters
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
RITE AID
NDC Product
Human Otc DrugAllergy Relief-d NDC 11822-9994
- Generic Name
- Cetirizine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rising Pharma Holdings, Inc.
NDC Product
Human Prescription DrugClomipramine Hydrochloride NDC 16571-683
- Generic Name
- Clomipramine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClomipramine Hydrochloride NDC 16571-684
- Generic Name
- Clomipramine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClomipramine Hydrochloride NDC 16571-685
- Generic Name
- Clomipramine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGabapentin NDC 16571-867
- Generic Name
- Gabapentin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGabapentin NDC 16571-868
- Generic Name
- Gabapentin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGabapentin NDC 16571-869
- Generic Name
- Gabapentin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
SUNRISE PHARMACEUTICAL, INC.
NDC Product
Human Prescription DrugPhentermine Hydrochloride NDC 11534-157
- Generic Name
- Phentermine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhentermine Hydrochloride NDC 11534-159
- Generic Name
- Phentermine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhentermine Hydrochloride NDC 11534-176
- Generic Name
- Phentermine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sandoz Inc
NDC Product
Human Prescription DrugAmoxicillin NDC 0781-2020
- Generic Name
- Amoxicillin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMycophenolate Mofetil NDC 0781-2067
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugButalbital, Aspirin, And Caffeine NDC 0781-2270
- Generic Name
- Butalbital, Aspirin, And Caffeine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0781-2299
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0781-2476
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0781-2477
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0781-2478
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0781-2479
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0781-2480
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0781-2481
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNintedanib NDC 0781-2492
- Generic Name
- Nintedanib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNintedanib NDC 0781-2495
- Generic Name
- Nintedanib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0781-2613
- Generic Name
- Amoxicillin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0781-5061
- Generic Name
- Amoxicillin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMycophenolate Mofetil NDC 0781-5175
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0781-6039
- Generic Name
- Amoxicillin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0781-6041
- Generic Name
- Amoxicillin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0781-6156
- Generic Name
- Amoxicillin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0781-6157
- Generic Name
- Amoxicillin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sandoz Inc.
NDC Product
Human Prescription DrugTacrolimus NDC 0781-2102
- Generic Name
- Tacrolimus
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTacrolimus NDC 0781-2103
- Generic Name
- Tacrolimus
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTacrolimus NDC 0781-2104
- Generic Name
- Tacrolimus
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Seton Pharmaceuticals LLC
NDC Product
Human Prescription DrugButalbital, Acetaminophen And Caffeine NDC 13925-535
- Generic Name
- Butalbital, Acetaminophen And Caffeine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugButalbital, Acetaminophen And Caffeine NDC 13925-536
- Generic Name
- Butalbital, Acetaminophen And Caffeine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
SpecGx LLC
NDC Product
Human Prescription DrugDextroamphetamine Sulfate Extended-release NDC 0406-8960
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Sulfate Extended-release NDC 0406-8961
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Sulfate Extended-release NDC 0406-8962
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRestoril NDC 0406-9914
- Generic Name
- Temazepam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRestoril NDC 0406-9915
- Generic Name
- Temazepam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRestoril NDC 0406-9916
- Generic Name
- Temazepam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRestoril NDC 0406-9917
- Generic Name
- Temazepam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemazepam NDC 0406-9959
- Generic Name
- Temazepam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTemazepam NDC 0406-9960
- Generic Name
- Temazepam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
TARGET CORPORATION
NDC Product
Human Otc DrugAcetaminophen NDC 11673-167
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
TARGET Corporation
NDC Product
Human Otc DrugStool Softener Laxative NDC 11673-341
- Generic Name
- Docusate Sodium
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Drug For Further Processing- Generic Name
- Mexiletine Hydrochloride
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugMexiletine Hydrochloride NDC 0093-8739
- Generic Name
- Mexiletine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMexiletine Hydrochloride NDC 0093-8740
- Generic Name
- Mexiletine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Mexiletine Hydrochloride
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Mexiletine Hydrochloride
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugMexiletine Hydrochloride NDC 0093-8741
- Generic Name
- Mexiletine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugMesalamine NDC 0480-7750
- Generic Name
- Mesalamine
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Upsher-Smith Laboratories, LLC
NDC Product
Human Prescription DrugIsotretinoin NDC 0832-8301
- Generic Name
- Isotretinoin
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsotretinoin NDC 0832-8302
- Generic Name
- Isotretinoin
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsotretinoin NDC 0832-8303
- Generic Name
- Isotretinoin
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsotretinoin NDC 0832-8304
- Generic Name
- Isotretinoin
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREEN CO.
NDC Product
Human Otc DrugAcetaminophen NDC 0363-9798
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAcetaminophen Diphenhydramine Hcl NDC 0363-9799
- Generic Name
- Acetaminophen Diphenhydramine Hcl
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
WALGREENS CO.
NDC Product
Human Otc DrugAcetaminophen Diphenhydramine Hcl NDC 0363-9664
- Generic Name
- Acetaminophen Diphenhydramine Hcl
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreen Company
NDC Product
Human Otc DrugWal-zyr D NDC 0363-0989
- Generic Name
- Cetirizine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreens
NDC Product
Human Otc DrugStool Softener Laxative NDC 0363-4100
- Generic Name
- Docusate Sodium
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugStool Softener Laxative NDC 0363-4202
- Generic Name
- Docusate Sodium
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreens Company
NDC Product
Human Otc DrugOmeprazole NDC 0363-1607
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
