NDC Product
Human Prescription DrugCephalexin NDC 42291-006
- Generic Name
- Cephalexin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Fd&c Blue No. 2 Aluminum Lake, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 4AQJ3LG584.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 15792-65-1 and the RxNorm Concept ID (RxCUI) 1307695. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
FD&C BLUE NO. 2 ALUMINUM LAKE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
4AQJ3LG584
The specific atomic composition represented as a molecular structure string.
InChIKey
3C16H8N2O8S2.2Al International Chemical Identifier digital signature for unique molecular identification.
SMILES String
LUMBYZCQSBZRHR-ZZAMBAHZSA-H 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
C/1(=C\2/Nc3ccc(S(=O)(=O)[O-])cc3C2=O)\Nc4ccc(S(=O)(=O)[O-])cc4C1=O.[Al+3].C/1(=C\2/Nc3c(C2=O)cc(S(=O)(=O)[O-])cc3)\Nc4c(C1=O)cc(S(=O)(=O)[O-])cc4.C/1(=C\2/Nc3c(C2=O)cc(S(=O)(=O)[O-])cc3)\Nc4c(C1=O)cc(S(=O)(=O)[O-])cc4.[Al+3]
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Fd&c Blue No. 2 Aluminum Lake. 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.
Common Names & Synonyms
C.I. FOOD BLUE 1-ALUMINUM LAKE
CN
DYE FDC BLUE NO. 2 ALUMINIUM LAKE
CN
FD&C BLUE NO. 2 ALUMINUM LAKE
CN
FD&C BLUE NO. 2--ALUMINIUM LAKE
CN
FD&C BLUE NO. 2--ALUMINUM LAKE
CN
NDC Products Containing FD&C BLUE NO. 2 ALUMINUM LAKE
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
AVKARE
Active Listing
NDC Product
Human Prescription DrugCephalexin NDC 42291-007
- Generic Name
- Cephalexin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Actavis Pharma, Inc.
NDC Product
Human Prescription DrugIsotretinoin NDC 0591-2435
- Generic Name
- Isotretinoin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsotretinoin NDC 0591-2436
- Generic Name
- Isotretinoin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsotretinoin NDC 0591-2451
- Generic Name
- Isotretinoin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsotretinoin NDC 0591-2501
- Generic Name
- Isotretinoin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
AiPing Pharmaceutical, Inc.
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 11788-077
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 11788-078
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 11788-079
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 11788-080
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 11788-081
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 11788-082
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLosartan Potassium NDC 11788-100
- Generic Name
- Losartan Potassium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLosartan Potassium NDC 11788-101
- Generic Name
- Losartan Potassium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLosartan Potassium NDC 11788-102
- Generic Name
- Losartan Potassium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin NDC 11788-132
- Generic Name
- Rosuvastatin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRosuvastatin NDC 11788-133
- Generic Name
- Rosuvastatin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Ajanta Pharma USA Inc.
NDC Product
Human Prescription DrugDoxepin NDC 27241-281
- Generic Name
- Doxepin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alembic Pharmaceuticals Limited
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 46708-725
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 46708-726
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 46708-727
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 46708-728
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 46708-729
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugChlorpromazine NDC 46708-737
- Generic Name
- Chlorpromazine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugChlorpromazine NDC 46708-738
- Generic Name
- Chlorpromazine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugChlorpromazine NDC 46708-739
- Generic Name
- Chlorpromazine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGuanfacine NDC 46708-747
- Generic Name
- Guanfacine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGuanfacine NDC 46708-748
- Generic Name
- Guanfacine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 46708-768
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 46708-789
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 46708-790
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 46708-791
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Amerisource Bergen
NDC Product
Human Otc DrugGentle Laxative NDC 46122-767
- Generic Name
- Bisacodyl
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Apnar Pharma LP
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 24689-119
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 24689-120
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvKARE
NDC Product
Human Prescription DrugCefdinir NDC 42291-043
- Generic Name
- Cefdinir
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEplerenone NDC 42291-454
- Generic Name
- Eplerenone
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEplerenone NDC 42291-455
- Generic Name
- Eplerenone
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbidopa And Levodopa NDC 42291-471
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbidopa And Levodopa NDC 42291-488
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 42291-901
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 42291-902
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 42291-903
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 42291-904
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisperidone NDC 42291-908
- Generic Name
- Risperidone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRisperidone NDC 42291-912
- Generic Name
- Risperidone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 42291-955
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 42291-956
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 42291-957
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 42291-958
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Belmora LLC
NDC Product
Human Otc DrugFlanax Pain Reliever/fever Reducer NDC 27854-505
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Better Living Brands, LLC
NDC Product
Human Otc DrugNaproxen NDC 21130-674
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNaproxen Sodium NDC 21130-856
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bi-Mart
NDC Product
Human Otc DrugNaproxen Sodium NDC 37835-594
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugMilnacipran Hydrochloride NDC 31722-846
- Generic Name
- Milnacipran Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMilnacipran Hydrochloride NDC 31722-847
- Generic Name
- Milnacipran Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMilnacipran Hydrochloride NDC 31722-848
- Generic Name
- Milnacipran Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMilnacipran Hydrochloride NDC 31722-849
- Generic Name
- Milnacipran Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMilnacipran Hydrochloride NDC 31722-880
- Generic Name
- Milnacipran Hydrochloride
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFingolimod NDC 31722-889
- Generic Name
- Fingolimod
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAripiprazole NDC 31722-919
- Generic Name
- Aripiprazole
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAripiprazole NDC 31722-920
- Generic Name
- Aripiprazole
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAripiprazole NDC 31722-921
- Generic Name
- Aripiprazole
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAripiprazole NDC 31722-922
- Generic Name
- Aripiprazole
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAripiprazole NDC 31722-923
- Generic Name
- Aripiprazole
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAripiprazole NDC 31722-924
- Generic Name
- Aripiprazole
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Church & Dwight Co., Inc.
NDC Product
Human Otc DrugZicam Cold And Flu-like Symptoms Echinacea Plus Sambucus NDC 10237-479
- Generic Name
- Zinc Acetate Anhydrous, Zinc Gluconate, Echinacea Angustifol...
- Dosage Form
- Tablet, Multilayer
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Cintas Corporation
NDC Product
Human Otc DrugFirst Aid Direct All Day Pain Relief NDC 42961-122
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cranbury Pharmaceuticals, LLC
NDC Product
Human Prescription DrugLevetiracetam NDC 27808-263
- Generic Name
- Levetiracetam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevetiracetam NDC 27808-264
- Generic Name
- Levetiracetam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevetiracetam NDC 27808-265
- Generic Name
- Levetiracetam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevetiracetam NDC 27808-266
- Generic Name
- Levetiracetam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Epic Pharma, LLC
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 42806-413
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugTums Chewy Bites Raspberry Lemonade NDC 0135-0188
- Generic Name
- Calcium Carbonate
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPanadol Cold And Flu Night NDC 0135-7034
- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hb...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNicorette Peppermint NDC 0135-8050
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Peppermint NDC 0135-8060
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
NDC Product
Human Prescription DrugTerazosin NDC 23155-735
- Generic Name
- Terazosin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTerazosin NDC 23155-736
- Generic Name
- Terazosin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTerazosin NDC 23155-737
- Generic Name
- Terazosin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTerazosin NDC 23155-738
- Generic Name
- Terazosin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline NDC 23155-757
- Generic Name
- Sertraline
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline NDC 23155-758
- Generic Name
- Sertraline
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline NDC 23155-759
- Generic Name
- Sertraline
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
HyVee Inc
NDC Product
Human Otc DrugOmeprazole NDC 42507-414
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAllergy Relief NDC 42507-847
- Generic Name
- Fexofenadine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Sleep Aid Ultra NDC 0113-4032
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lannett Company, Inc
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 0527-3280
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 0527-3282
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 0527-3283
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 0527-3284
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 0527-3285
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 0527-3286
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 0527-3287
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 0527-3288
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 0527-3289
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 0527-3290
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugLevothyroxine Sodium NDC 0527-3291
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Lannett Company, Inc.
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0527-0790
- Generic Name
- Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0527-0791
- Generic Name
- Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0527-0792
- Generic Name
- Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0527-0793
- Generic Name
- Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0527-0794
- Generic Name
- Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0527-0795
- Generic Name
- Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
- Dosage Form
- Capsule, Extended Release
- 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
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0527-4661
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0527-4662
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0527-4663
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0527-4664
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0527-4665
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0527-4666
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0527-4667
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Laurus Labs Limited
NDC Product
Human Prescription DrugOseltamivir NDC 42385-985
- Generic Name
- Oseltamivir Phosphate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOseltamivir NDC 42385-986
- Generic Name
- Oseltamivir Phosphate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOseltamivir NDC 42385-987
- Generic Name
- Oseltamivir Phosphate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Macleods Pharmaceuticals Limited
NDC Product
Human Prescription DrugLacosamide NDC 33342-302
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLacosamide NDC 33342-303
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLacosamide NDC 33342-304
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLacosamide NDC 33342-305
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Major Pharmaceuticals
NDC Product
Human Prescription DrugEnalapril Maleate NDC 0904-7311
- Generic Name
- Enalapril Maleate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEnalapril Maleate NDC 0904-7312
- Generic Name
- Enalapril Maleate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Sr NDC 0904-7465
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNebivolol NDC 0904-7497
- Generic Name
- Nebivolol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNebivolol NDC 0904-7498
- Generic Name
- Nebivolol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNebivolol NDC 0904-7499
- Generic Name
- Nebivolol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCelecoxib NDC 0904-7550
- Generic Name
- Celecoxib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCelecoxib NDC 0904-7551
- Generic Name
- Celecoxib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 0904-7593
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 0904-7594
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxcarbazepine NDC 0904-7595
- Generic Name
- Oxcarbazepine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Marlex Pharmaceuticals, Inc
NDC Product
Human Prescription DrugLacosamide NDC 10135-799
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLacosamide NDC 10135-800
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLacosamide NDC 10135-801
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLacosamide NDC 10135-802
- Generic Name
- Lacosamide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugWelireg NDC 0006-5331
- Generic Name
- Belzutifan
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 0615-8582
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugVelsipity NDC 0069-0274
- Generic Name
- Etrasimod
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugXeljanz Xr NDC 0069-0502
- Generic Name
- Tofacitinib
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugXeljanz NDC 0069-1029
- Generic Name
- Tofacitinib
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
QPharma, Inc.
NDC Product
Human Prescription DrugOmeprazole NDC 42708-158
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rite Aid Corporation
NDC Product
Human Otc DrugBack And Muscle Pain NDC 11822-4170
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNaproxen Sodium NDC 11822-4171
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugCold And Flu Severe, Daytime, Nighttime NDC 11822-5034
- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hb...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSinus Relief Daytime, Nighttime NDC 11822-5694
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Guaifenesin, Phenylephri...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNaproxen Sodium NDC 11822-6040
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
SAFEWAY
NDC Product
Human Otc DrugNaproxen Sodium Diphenhydramine Hydrochloride NDC 21130-814
- Generic Name
- Naproxen Sodium Diphenhydramine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Safeway
NDC Product
Human Otc DrugNaproxen Sodium NDC 21130-593
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugIbuprofen Pm NDC 21130-623
- Generic Name
- Diphenhydramine Citrate, Ibuprofen
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNaproxen Sodium Pm NDC 21130-639
- Generic Name
- Diphenhydramine Hydrochloride, Naproxen Sodium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sandoz Inc.
NDC Product
Human Prescription DrugPrucalopride NDC 0781-8159
- Generic Name
- Prucalopride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Solco Healthcare US,LLC
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 43547-602
- Generic Name
- Lisdexamfetamine Dimesylate Capsules
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 43547-603
- Generic Name
- Lisdexamfetamine Dimesylate Capsules
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 43547-604
- Generic Name
- Lisdexamfetamine Dimesylate Capsules
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 43547-605
- Generic Name
- Lisdexamfetamine Dimesylate Capsules
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 43547-606
- Generic Name
- Lisdexamfetamine Dimesylate Capsules
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 43547-607
- Generic Name
- Lisdexamfetamine Dimesylate Capsules
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 43547-608
- Generic Name
- Lisdexamfetamine Dimesylate Capsules
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 43547-634
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
TARGET CORPORATION
NDC Product
Human Otc DrugNaproxen Sodium And Diphenhydramine Hcl NDC 11673-819
- Generic Name
- Naproxen Sodium And Diphenhydramine Hcl
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
TOPCO ASSOCIATES LLC
NDC Product
Human Otc DrugLaxative Docusate Sodium With Senna NDC 36800-861
- Generic Name
- Docusate Sodium And Sennosides
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Target Corporation
NDC Product
Human Otc DrugDaytime Nighttime Sinus Relief NDC 11673-282
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Guaifenesin, Phenylephri...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Drug For Further Processing- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugAcitretin NDC 0093-1135
- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcitretin NDC 0093-1136
- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugAcitretin NDC 0093-1138
- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 0093-8199
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 0093-8224
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 0093-8229
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSunitinib Malate NDC 0093-8231
- Generic Name
- Sunitinib Malate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbidopa And Levodopa NDC 0093-9701
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbidopa And Levodopa NDC 0093-9702
- Generic Name
- Carbidopa And Levodopa
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugVilazodone Hydrochloride NDC 0480-2043
- Generic Name
- Vilazodone Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTopiramate NDC 0480-2359
- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugFerric Citrate NDC 0480-2996
- Generic Name
- Ferric Citrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPerampanel NDC 0480-7066
- Generic Name
- Perampanel
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPerampanel NDC 0480-7067
- Generic Name
- Perampanel
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPerampanel NDC 0480-7068
- Generic Name
- Perampanel
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Topco Associates, LLC
NDC Product
Human Otc DrugSleep Aid NDC 36800-672
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMenstrual Relief Maximum Strength NDC 36800-979
- Generic Name
- Acetaminophen, Pamabrom, Pyrilamine Maleate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Unichem Pharmaceuticals (USA), Inc.
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 29300-421
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 29300-422
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 29300-423
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmitriptyline Hydrochloride NDC 29300-424
- Generic Name
- Amitriptyline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
United Natural Foods, Inc. dba UNFI
NDC Product
Human Otc DrugDaytime Cold, Nighttime Cold Multi-symptom NDC 41163-529
- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hb...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGentle Laxative NDC 41163-607
- Generic Name
- Bisacodyl
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Upsher-Smith Laboratories, LLC
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 24979-137
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 24979-138
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 24979-139
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREENS
NDC Product
Human Otc DrugAll Day Pain Relief NDC 0363-9608
- Generic Name
- Naproxen Sodium
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreen Company
NDC Product
Human Otc DrugAll Night Pain Relief Pm NDC 0363-2264
- Generic Name
- Diphenhydramine Hydrochloride, Naproxen Sodium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSleep Aid NDC 0363-3462
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSleep Aid NDC 0363-6720
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
e5 Pharma, LLC
NDC Product
Human Prescription DrugNitazoxanide NDC 13517-135
- Generic Name
- Nitazoxanide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
