NDC Product
Human Prescription DrugHumira NDC 0074-0124
- Generic Name
- Adalimumab
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- BLA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Isopropyl Alcohol, uniquely identified by the FDA Unique Ingredient Identifier (UNII) ND2M416302.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 67-63-0 and the RxNorm Concept ID (RxCUI) 797541. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
ISOPROPYL ALCOHOL
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
ND2M416302
The specific atomic composition represented as a molecular structure string.
InChIKey
C3H8O International Chemical Identifier digital signature for unique molecular identification.
SMILES String
KFZMGEQAYNKOFK-UHFFFAOYSA-N Line notation for describing the chemical structure and connectivity of atoms.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
OC(C)C
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Isopropyl 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
ISOPROPYL ALCOHOL
OF
Common Names & Synonyms
2-PROPANOL [USP-RS]
CN
2-PROPANOL [WHO-IP]
CN
2-PROPANOLUM [WHO-IP LATIN]
CN
ACETONE IMPURITY B [EP IMPURITY]
CN
ALCOHOL,ISOPROPYL
CN
ALCOHOL,ISOPROPYL [VANDF]
CN
CHLORAPREP COMPONENT ISOPROPYL ALCOHOL
CN
DURAPREP COMPONENT ISOPROPYL ALCOHOL
CN
ISOPROPANOL [JAN]
CN
ISOPROPANOL [WHO-DD]
CN
ISOPROPYL ALCOHOL [EP MONOGRAPH]
CN
ISOPROPYL ALCOHOL [FCC]
CN
ISOPROPYL ALCOHOL [FHFI]
CN
ISOPROPYL ALCOHOL [HSDB]
CN
ISOPROPYL ALCOHOL [IARC]
CN
ISOPROPYL ALCOHOL [II]
CN
ISOPROPYL ALCOHOL [MART.]
CN
ISOPROPYL ALCOHOL [MI]
CN
ISOPROPYL ALCOHOL [ORANGE BOOK]
CN
ISOPROPYL ALCOHOL [USP MONOGRAPH]
CN
ISOPROPYL ALCOHOL [VANDF]
CN
Brand / Trade Names
SOLUPREP COMPONENT ISOPROPYL ALCOHOL
BN
ZURAGARD
BN
Systematic Nomenclature
2-PROPANOL
SYS
ALCOHOL, ISOPROPYL
SYS
ISOPROPANOL
SYS
ISOPROPYL ALCOHOL (ISOPROPANOL)
SYS
Technical Codes
FEMA NO. 2929
CD
NSC-135801
CD
NDC Products Containing ISOPROPYL 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
NDC Product
Human Prescription DrugHumira NDC 0074-0243
- Generic Name
- Adalimumab
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumira NDC 0074-0554
- Generic Name
- Adalimumab
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumira NDC 0074-0616
- Generic Name
- Adalimumab
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumira NDC 0074-0817
- Generic Name
- Adalimumab
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- BLA
Active Listing
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
NDC Product
Human Prescription DrugHumira NDC 0074-1539
- Generic Name
- Adalimumab
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugLupron Depot-ped NDC 0074-2108
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLupron Depot-ped NDC 0074-2282
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLupron Depot-ped NDC 0074-2440
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugHumira NDC 0074-2540
- Generic Name
- Adalimumab
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugLupron Depot NDC 0074-3346
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLupron Depot NDC 0074-3473
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLupron Depot NDC 0074-3641
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLupron Depot NDC 0074-3642
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLupron Depot NDC 0074-3683
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLupron Depot-ped NDC 0074-3779
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugHumira NDC 0074-3799
- Generic Name
- Adalimumab
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHumira NDC 0074-4339
- Generic Name
- Adalimumab
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugLupron Depot-ped NDC 0074-9694
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
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
American Regent, Inc.
NDC Product
Human Prescription DrugBetamethasone Sodium Phosphate And Betamethasone Acetate NDC 0517-0720
- Generic Name
- Betamethasone Sodium Phosphate And Betamethasone Acetate
- Dosage Form
- Injection, Suspension
- Route
- Intra-articular; Intralesional; Intramuscular
- 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
Bausch Health US, LLC
NDC Product
Human Prescription DrugMestinon NDC 0187-3013
- Generic Name
- Pyridostigmine Bromide
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Bayer HealthCare LLC
NDC Product
Human Otc DrugAleve Arthritis Pain Gel NDC 0280-0039
- Generic Name
- Diclofenac Sodium
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- ANDA
Active Listing
Crown Laboratories
NDC Product
Human Otc DrugMineral Ice Pain Relieving NDC 0316-0226
- Generic Name
- Menthol
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC
NDC Product
Human Prescription DrugBetamethasone Valerate NDC 0168-0041
- Generic Name
- Betamethasone Valerate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBetamethasone Dipropionate NDC 0168-0057
- Generic Name
- Betamethasone Dipropionate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClindamycin Phosphate NDC 0168-0201
- Generic Name
- Clindamycin Phosphate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClindamycin Phosphate NDC 0168-0202
- Generic Name
- Clindamycin Phosphate
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBetamethasone Dipropionate NDC 0168-0267
- Generic Name
- Betamethasone Dipropionate
- Dosage Form
- Lotion, Augmented
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClobetasol Propionate NDC 0168-0269
- Generic Name
- Clobetasol Propionate
- Dosage Form
- Solution
- Route
- Topical
- 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
Fougera Pharmaceuticals, LLC
NDC Product
Human Otc DrugSwim-ear NDC 0168-0126
- Generic Name
- Swim-ear
- Dosage Form
- Solution
- Route
- Auricular (otic)
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Galderma Laboratories, L.P.
NDC Product
Human Otc DrugCetaphil Gentle Clear Clarifying Acne Cleanser NDC 0299-4119
- Generic Name
- Salicylic Acid
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
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 DrugExcedrin Extra Strength Geltabs NDC 0067-2021
- Generic Name
- Acetaminophen, Asprin, Caffeine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Migraine Geltabs NDC 0067-2035
- Generic Name
- Acetaminophen, Asprin, Caffeine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugVoltaren Arthritis Pain NDC 0067-8152
- Generic Name
- Diclofenac Sodium
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugVoltaren Arthritis Pain NDC 0067-8153
- Generic Name
- Diclofenac Sodium
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
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
Henry Schein Inc.
NDC Product
Human Otc DrugIsopropyl Rubbing Alcohol NDC 0404-0002
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlcohol Prep Pad Large Pad NDC 0404-9406
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Cloth
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlcohol Prep Pad Medium Pad NDC 0404-9407
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Cloth
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlcohol Prep Pad Medium Pad NDC 0404-9408
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Cloth
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Henry Schein, Inc.
NDC Product
Human Otc DrugAlcohol Prep Pads NDC 0404-0007
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Swab
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlcohol Prep Pads NDC 0404-0103
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Swab
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMaxiclens Chlorhexidine Gluconate Liquid Solution, 4% NDC 0404-0219
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugMaxiclens Chlorhexidine Gluconate Liquid Solution, 4% NDC 0404-0220
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugMaxiclens Chlorhexidine Gluconate Liquid Solution, 4% NDC 0404-0221
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- NDA
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 DrugIcosapent Ethyl NDC 0054-0508
- Generic Name
- Icosapent Ethyl
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Humco Holding Group, Inc.
NDC Product
Human Otc DrugHumco Ear Drops For Swimmers NDC 0395-0098
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Liquid
- Route
- Auricular (otic)
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugHumco 1 Percent Iodine NDC 0395-1211
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugHumco Isopropyl Rubbing Alcohol 70% NDC 0395-1249
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugHumco Isopropyl Rubbing Alcohol 70% Professional Pack NDC 0395-4202
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
L Perrigo Company
NDC Product
Human Otc DrugMederma Pm NDC 0113-4124
- Generic Name
- Dimethicone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Ibuprofen NDC 0113-0298
- Generic Name
- Ibuprofen
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Arthritis Pain NDC 0113-1189
- Generic Name
- Diclofenac Sodium
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Lice Killing Creme Rinse NDC 0113-1910
- Generic Name
- Permethrin
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Ibuprofen NDC 0113-4501
- Generic Name
- Ibuprofen
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Arthritis Pain NDC 0113-8175
- Generic Name
- Diclofenac Sodium
- Dosage Form
- Gel
- Route
- Topical
- 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 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, 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 DrugDronabinol NDC 0527-4125
- Generic Name
- Dronabinol
- 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
Molnlycke Health Care
NDC Product
Human Otc DrugHibiclens NDC 0234-0575
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugHibiclens NDC 0234-0575
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugHibiclens NDC 0234-0575
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- NDA
Active Listing
PAI Holdings, LLC dba PAI Pharma
NDC Product
Human Prescription DrugLeuprolide Acetate NDC 0121-2106
- Generic Name
- Leuprolide Acetate
- Dosage Form
- Kit
- Route
- Subcutaneous
- Marketing
- ANDA
Active Listing
Parke-Davis Div of Pfizer Inc
NDC Product
Human Prescription DrugNardil NDC 0071-0350
- Generic Name
- Phenelzine Sulfate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugAbrilada NDC 0025-0325
- Generic Name
- Adalimumab-afzb
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugAbrilada NDC 0025-0328
- Generic Name
- Adalimumab-afzb
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugAbrilada NDC 0025-0333
- Generic Name
- Adalimumab-afzb
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugVyndamax NDC 0069-8730
- Generic Name
- Tafamidis
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
Pharmacia & Upjohn Company LLC
NDC Product
Human Prescription DrugCleocin T NDC 0009-3329
- Generic Name
- Clindamycin Phosphate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- NDA
Active Listing
Rugby Laboratories
NDC Product
Human Otc DrugRugby Ice Blue External Analgesic NDC 0536-1061
- Generic Name
- Menthol, Unspecified Form
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
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 0406-9916
- 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
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugNystatin NDC 0093-0983
- Generic Name
- Nystatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Nystatin
- Dosage Form
- Tablet, Film Coated
- 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
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 0093-8740
- Generic Name
- Mexiletine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
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 DrugVigadrone NDC 0245-6001
- Generic Name
- Vigabatrin
- Dosage Form
- Tablet
- 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
WALGREEN COMPANY
NDC Product
Human Otc DrugWalgreens Cooling NDC 0363-0954
- Generic Name
- Lidocaine Hydrochloride
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
WALGREENS
NDC Product
Human Otc DrugArnica Gel NDC 0363-0139
- Generic Name
- Arnica
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
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
NDC Product
Human Otc DrugWalgreens NDC 0363-5721
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreen Co.
NDC Product
Human Otc DrugOvernight Cold Therapy Pain Relief NDC 0363-0355
- Generic Name
- Menthol, Unspecified Form
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCold Therapy Pain Relief NDC 0363-0356
- Generic Name
- Menthol, Unspecified Form
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreens 70% Isopropyl Alcohol NDC 0363-0380
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFree And Pure Cold Therapy Pain Relief NDC 0363-0383
- Generic Name
- Menthol
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug70% NDC 0363-0810
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAntiseptic Skin Cleanser NDC 0363-1061
- Generic Name
- Chlorhexidine Gluconate 4%
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- NDA
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
NDC Product
Human Otc DrugArthritis Pain Relieving NDC 0363-3003
- Generic Name
- Diclofenac Sodium
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugArthritis Pain Relieving NDC 0363-5123
- Generic Name
- Diclofenac Sodium
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugWalgreens Ice Blue Pain Relieving Topical Analgesic NDC 0363-6330
- Generic Name
- Menthol, Unspecified Form
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreens 70% Isopropyl Alcohol Wipes NDC 0363-6505
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Cloth
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreens Scalp Relief External Analgesic NDC 0363-9068
- Generic Name
- Hydrocortisone
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreens
NDC Product
Human Otc DrugIsopropyl Alcohol 70 Percent NDC 0363-0275
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugIsopropyl Alcohol 91 Percent NDC 0363-0277
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugIsopropyl Alcohol 70 Percent NDC 0363-0472
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreens NDC 0363-0859
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreens NDC 0363-1233
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugWalgreens Arnica NDC 0363-3034
- Generic Name
- Arnica Montana 7%
- Dosage Form
- Aerosol, Spray
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
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
NDC Product
Human Otc DrugWalgreens NDC 0363-5721
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreens Co
NDC Product
Human Otc DrugWalgreens Swimmers Ear NDC 0363-6107
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreens Co.
NDC Product
Human Otc DrugWalgreens 91% Isopropyl Alcohol NDC 0363-0381
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugIsopropyl Alcohol NDC 0363-0804
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug70% Rubbing NDC 0363-0845
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreens Company
NDC Product
Human Otc DrugWalgreen Alcohol NDC 0363-0809
- Generic Name
- Isopropyl Alcohol
- Dosage Form
- Swab
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDiclofenac Sodium Topical Gel 1% NDC 0363-7065
- Generic Name
- Diclofenac Sodium Topical Gel, 1%
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- ANDA
Active Listing
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
NDC Product
Human Prescription DrugDuavee NDC 0008-1123
- Generic Name
- Conjugated Estrogens/bazedoxifene
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Xttrium Laboratories, Inc.
NDC Product
Human Otc DrugCardinal Health NDC 0116-0061
- Generic Name
- Chlorhexidine Gluconate 4%
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAntiseptic Skin Cleanser NDC 0116-0161
- Generic Name
- Chlorhexidine Gluconate 4%
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBetasept NDC 0116-0200
- Generic Name
- Antiseptic Surgical Scrub
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAntiseptic Skin Cleanser NDC 0116-0767
- Generic Name
- Chlorhexidine Gluconate 4%
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugCliniclean NDC 0116-0901
- Generic Name
- Chlorhexidine Gluconate 4%
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugDyna-hex 2 NDC 0116-1021
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugDyna-hex 2 NDC 0116-1022
- Generic Name
- Chlorhexidine Gluconate 2%
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugDyna-hex 2 NDC 0116-1022
- Generic Name
- Chlorhexidine Gluconate 2%
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugDyna-hex 4 NDC 0116-1060
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugDyna-hex 4 NDC 0116-1060
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAntiseptic Skin Cleanser NDC 0116-1061
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAntiseptic Skin Cleanser NDC 0116-1061
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAntiseptic Skin Cleanser NDC 0116-1061
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugBactoshield Chg NDC 0116-1344
- Generic Name
- Chlorhexidine Gluconate
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugProvon Antimicrobial Foam Handwash NDC 0116-8500
- Generic Name
- Chlorhexidine Gluconate 2%
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- NDA
Active Listing
