NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 50090-0928
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Succinic Acid, uniquely identified by the FDA Unique Ingredient Identifier (UNII) AB6MNQ6J6L.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 110-15-6 and the RxNorm Concept ID (RxCUI) 37255. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
SUCCINIC ACID
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
AB6MNQ6J6L
The specific atomic composition represented as a molecular structure string.
InChIKey
C4H6O4 International Chemical Identifier digital signature for unique molecular identification.
SMILES String
KDYFGRWQOYBRFD-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
C(CC(=O)O)C(=O)O
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Succinic Acid. 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
SUCCINIC ACID
OF
Common Names & Synonyms
ADIPIC ACID IMPURITY B [EP IMPURITY]
CN
AMBER ACID
CN
DIHYDROFUMARIC ACID
CN
SUCCINIC ACID [FCC]
CN
SUCCINIC ACID [HSDB]
CN
SUCCINIC ACID [II]
CN
SUCCINIC ACID [MART.]
CN
SUCCINIC ACID [MI]
CN
SUCCINIC ACID [USP IMPURITY]
CN
SUCCINIC ACID [USP-RS]
CN
SUCCINIC ACID [VANDF]
CN
SUCCINIC ACID [WHO-DD]
CN
SUCCINICUM ACIDUM
CN
SUCCINICUM ACIDUM [HPUS]
CN
Systematic Nomenclature
1,2-ETHANEDICARBOXYLIC ACID
SYS
BUTANEDIOIC ACID
SYS
Technical Codes
FEMA NO. 4719
CD
NSC-106449
CD
NDC Products Containing SUCCINIC ACID
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 (250), only Active Listings are currently displayed.
Showing 186 active products
A-S Medication Solutions
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 50090-1857
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 50090-2219
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 50090-3309
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 50090-5873
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 50090-5932
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 50090-6222
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 50090-6694
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHadlima NDC 50090-6707
- Generic Name
- Adalimumab-bwwd
- Dosage Form
- Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
Allegis Holdings, LLC
NDC Product
Human Prescription DrugAugmentin NDC 71297-240
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
Amazon.com Services LLC
NDC Product
Human Otc DrugBasic Care Childrens Ibuprofen NDC 72288-461
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugBasic Care Childrens Ibuprofen NDC 72288-521
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugBasic Care Childrens Ibuprofen NDC 72288-763
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
American Health Packaging
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 60687-532
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 60687-543
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 60687-554
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 60687-565
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
American Sales Company
NDC Product
Human Otc DrugCareone Childrens Ibuprofen NDC 41520-633
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugCareone Childrens Ibuprofen NDC 41520-740
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Amerisource Bergen
NDC Product
Human Otc DrugGood Neighbor Pharmacy Childrens Ibuprofen NDC 46122-617
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Neighbor Pharmacy Childrens Ibuprofen NDC 46122-632
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Amgen, Inc
NDC Product
Human Prescription DrugParsabiv NDC 55513-740
- Generic Name
- Etelcalcetide
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugParsabiv NDC 55513-741
- Generic Name
- Etelcalcetide
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugParsabiv NDC 55513-742
- Generic Name
- Etelcalcetide
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
Amneal Pharmaceuticals LLC
NDC Product
Human Prescription DrugPyridostigmine Bromide NDC 60846-559
- Generic Name
- Pyridostigmine Bromide
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Array BioPharma Inc.
NDC Product
Human Prescription DrugBraftovi NDC 70255-025
- Generic Name
- Encorafenib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Asclemed USA, Inc.
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 76420-859
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 76420-864
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aurobindo Pharma Limited
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 59651-025
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 59651-026
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 65862-533
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 65862-534
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 65862-535
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvPAK
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 50268-545
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 50268-546
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 50268-547
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 50268-548
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Avion Pharmaceuticals, LLC
NDC Product
Human Prescription DrugNiferex NDC 75854-344
- Generic Name
- Ferrous Asparto Glycinate, Iron, Ascorbic Acid, Folic Acid, ...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Banuskin, Inc.
NDC Product
Human Otc DrugAha Bha Blemish Control And Exfoliating Serum NDC 85439-0101
- Generic Name
- Salicylic Acid Serum
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Brand Evangelists for Beauty Ltd
NDC Product
Human Otc DrugThe Inkey List Succinic Acid Acne Treatment NDC 81136-017
- Generic Name
- Salicylic Acid
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
CVS Pharmacy
NDC Product
Human Otc DrugChildrens Ibuprofen NDC 69842-329
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Ibuprofen NDC 69842-521
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 31722-952
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 31722-953
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 31722-954
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 31722-955
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cardinal Health 110, LLC. dba Leader
NDC Product
Human Otc DrugLeader Ibuprofen NDC 70000-0239
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Chartwell RX, LLC
NDC Product
Human Prescription DrugDiazepam NDC 62135-768
- Generic Name
- Diazepam Oral Solution (concentrate)
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Church & Dwight Co., Inc.
NDC Product
Human Otc DrugZicam Cold Remedy NDC 10237-472
- Generic Name
- Galphimia Glauca Flowering Top, Luffa Operculata Fruit, And ...
- Dosage Form
- Gel
- Route
- Nasal
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugZicam Cold Remedy NDC 10237-474
- Generic Name
- Galphimia Glauca Flowering Top, Luffa Operculata Fruit, And ...
- Dosage Form
- Spray
- Route
- Nasal
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Cordavis Limited
NDC Product
Human Prescription DrugAdalimumab-bwwd NDC 83457-186
- Generic Name
- Adalimumab-bwwd
- Dosage Form
- Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugAdalimumab-bwwd NDC 83457-187
- Generic Name
- Adalimumab-bwwd
- Dosage Form
- Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
Deseret Biologicals, Inc.
NDC Product
Human Otc DrugProstate NDC 43742-2092
- Generic Name
- Petroselinum Sativum, Populus Tremuloides, Sabal Serrulata, ...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugBio Co Enzyme Phase NDC 43742-2259
- Generic Name
- Aconiticum Acidum, Cis-, Adenosinum Triphosphoricum Dinatrum...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Direct_Rx
NDC Product
Human Prescription DrugAmoxicillin/clav Pot Oral Susp NDC 72189-367
- Generic Name
- Amoxicillin/clav Pot Oral Susp
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Distribuidora Comercial Jafra, S.A. de C.V.
NDC Product
Human Otc DrugClear Smart Clear Pore Hydrator NDC 68828-701
- Generic Name
- Salicylic Acid
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Dolgencorp, LLC
NDC Product
Human Otc DrugRexall Ibuprofen NDC 55910-521
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Energetix Corporation
NDC Product
Human Otc DrugThyro-chord NDC 64578-0076
- Generic Name
- Homeopathic Liquid
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Energique, Inc.
NDC Product
Human Otc DrugSpleenex Vh NDC 44911-0294
- Generic Name
- Aralia Quinquefolia, Ginkgo Biloba, Pancreas Suis, Spleen (s...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugLiverex I NDC 44911-0419
- Generic Name
- Ginkgo Biloba, Fel Tauri, Gallbladder (suis), Hepar Suis), T...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugLungex Ii NDC 44911-0439
- Generic Name
- Ginkgo Biloba, Colon (suis), Lung (suis), Pancreas Suis, Ger...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugSpleenex V NDC 44911-0539
- Generic Name
- Aralia Quinquefolia, Potassium Gluconate, Ginkgo Biloba, Mag...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugKidnex Iv NDC 44911-0747
- Generic Name
- Ginkgo Biloba, Alpha-ketoglutaricum Acidum, Citricum Acidum,...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Galderma Laboratories, L.P.
NDC Product
Human Otc DrugCetaphil Gentle Clear Triple-action Acne Serum NDC 0299-4135
- Generic Name
- Salicylic Acid
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Genentech, Inc.
NDC Product
Human Prescription DrugKadcyla NDC 50242-087
- Generic Name
- Ado-trastuzumab Emtansine
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugKadcyla NDC 50242-088
- Generic Name
- Ado-trastuzumab Emtansine
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugPolivy NDC 50242-103
- Generic Name
- Polatuzumab Vedotin
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugPolivy NDC 50242-105
- Generic Name
- Polatuzumab Vedotin
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- BLA
Active Listing
Golden State Medical Supply, Inc.
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 51407-924
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 51407-925
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 51407-926
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 51407-927
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Guna spa
NDC Product
Human Otc DrugOmeosport NDC 17089-075
- Generic Name
- .alpha.-ketoglutaric Acid - Aconitic Acid, Cis - Adenosine T...
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugGuna-kidney NDC 17089-298
- Generic Name
- Chondrodendron Tomentosum Root - Clerodendranthus Spicatus L...
- Dosage Form
- Solution/ Drops
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugGuna-allergy-prev NDC 17089-299
- Generic Name
- Ambrosia Artemisiifolia - Anguilla Rostrata Blood Serum - Ar...
- Dosage Form
- Solution/ Drops
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugGuna-cell NDC 17089-450
- Generic Name
- Acetylcarnitine, L-ampc-alpha-lipoic Ac-a-tocopherol-ascorbi...
- Dosage Form
- Solution/ Drops
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugGuna Osteo NDC 17089-473
- Generic Name
- Arnica Montana Root - Calcium Fluoride - Calcium Phosphate -...
- Dosage Form
- Solution/ Drops
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugAlprazolam NDC 0054-3068
- Generic Name
- Alprazolam
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiazepam Intensol NDC 0054-3185
- Generic Name
- Diazepam Intensol
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 0143-9853
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 0143-9981
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 0143-9982
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hinature Inc.
NDC Product
Human Otc DrugPurito Acne Intensive Treatment NDC 73251-011
- Generic Name
- Salicylic Acid
- Dosage Form
- Patch
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Horizon Therapeutics USA, Inc.
NDC Product
Human Prescription DrugActimmune NDC 75987-111
- Generic Name
- Interferon Gamma-1b
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
HyVee Inc
NDC Product
Human Otc DrugIbuprofen NDC 42507-461
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Janssen Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugConcerta NDC 50458-585
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugConcerta NDC 50458-586
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugConcerta NDC 50458-587
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugConcerta NDC 50458-588
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Jazz Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugZiihera NDC 68727-950
- Generic Name
- Zanidatamab-hrii
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- BLA
Active Listing
KOS� America, Inc.
NDC Product
Human Otc DrugDecorte Aq Absolute Treatment Awakening Protective Day NDC 66820-0500
- Generic Name
- Avobenzone, Octinoxate, Octisalate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Kenvue Brands LLC
NDC Product
Human Otc DrugChildrens Motrin NDC 50580-932
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Motrin NDC 50580-933
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNeutrogena Evenly Clear Acne Gel Moisturizer NDC 69968-0946
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNeutrogena Evenly Clear Acne Prone Skin Essentials NDC 69968-1005
- Generic Name
- Salicylic Acid
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
King Bio Inc.
NDC Product
Human Otc Drug911 Adrenal Burnout And Fatigue NDC 57955-9994
- Generic Name
- Aceticum Ac, Adrenalinum, Adrenocorticotrophin (30x), Aescul...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Kroger Company
NDC Product
Human Otc DrugChildrens Ibuprofen NDC 30142-402
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Ibuprofen NDC 30142-513
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Childrens Ibuprofen NDC 0113-2461
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Ibuprofen NDC 0113-6040
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Ibuprofen NDC 0113-7366
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Meijer Distribution Inc
NDC Product
Human Otc DrugChildrens Ibuprofen NDC 41250-331
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Ibuprofen NDC 41250-726
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Meijer, Inc.
NDC Product
Human Otc DrugChildrens Ibuprofen NDC 79481-0419
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Meitheal Pharmaceuticals Inc.
NDC Product
Human Prescription DrugContepo NDC 71288-035
- Generic Name
- Fosfomycin Disodium
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
Micro Labs Limited
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 42571-163
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 42571-164
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NorthStar Rx LLC
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 16714-292
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 16714-293
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 16714-294
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Northstar Rx LLC
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 72603-399
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NuCare Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 68071-3807
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NuCare Pharmaceuticals,Inc.
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 68071-1619
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 68071-2227
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 68071-2355
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 68071-2852
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 68071-5144
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 68071-5207
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Nutritional Specialties, Inc.
NDC Product
Human Otc DrugMetab NDC 83027-0116
- Generic Name
- Calcarea Sulphurica, Kali Muriaticum, Kali Phosphoricum, Kal...
- Dosage Form
- Spray
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Peace Out LLC.
NDC Product
Human Otc DrugPeace Out Early Stage Acne Dot NDC 71494-007
- Generic Name
- Salicylic Acid
- Dosage Form
- Patch
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugIbrance NDC 0069-0284
- Generic Name
- Palbociclib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZirabev NDC 0069-0315
- Generic Name
- Bevacizumab-bvzr
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugZirabev NDC 0069-0342
- Generic Name
- Bevacizumab-bvzr
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugIbrance NDC 0069-0486
- Generic Name
- Palbociclib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIbrance NDC 0069-0688
- Generic Name
- Palbociclib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZavzpret NDC 0069-3500
- Generic Name
- Zavegepant
- Dosage Form
- Spray
- Route
- Nasal
- Marketing
- NDA
Active Listing
Preferred Pharmaceuticals Inc.
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 68788-8299
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 68788-8306
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 68788-8318
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 68788-8770
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Preferred Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 68788-0483
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Proficient Rx LP
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 63187-826
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 71205-036
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 71205-462
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 82804-017
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Publix Super Markets Inc
NDC Product
Human Otc DrugChildrens Ibuprofen NDC 56062-801
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rael, Inc.
NDC Product
Human Otc DrugRael Beauty Miracle Clear Complete Acne Serum NDC 72863-109
- Generic Name
- Salicylic Acid
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rite Aid Corporation
NDC Product
Human Otc DrugChildrens Ibuprofen NDC 11822-1521
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Ibuprofen NDC 11822-4461
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
SOLARA SUNCARE, INC.
NDC Product
Human Otc DrugSolara Suncare - Fortune Teller Spf-30 NDC 73054-120
- Generic Name
- Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
SRL ENTERPRISES LLC
NDC Product
Human Otc DrugClearsynergy NDC 71617-100
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
SRL Enterprises, LLC
NDC Product
Human Otc DrugClearsynergy NDC 71617-102
- Generic Name
- Salicylic Acid
- Dosage Form
- Cloth
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Safeway
NDC Product
Human Otc DrugSignature Care Childrens Ibuprofen NDC 21130-701
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Ibuprofen NDC 21130-790
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sandoz Inc
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 0781-6102
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 0781-6104
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Source Naturals, Inc.
NDC Product
Human Otc DrugAllercetin NDC 64471-196
- Generic Name
- Euphrasia Officinalis, Kali Iodatum, Sabadilla, Sticta Pulmo...
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Strategic Sourcing Services LLC
NDC Product
Human Otc DrugFoster And Thrive Childrens Ibuprofen Ib NDC 70677-1145
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sun Pharmaceutical Industries, Inc.
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 57664-606
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 57664-607
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 57664-608
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 57664-609
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 57664-710
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
THG Beauty USA LLC
NDC Product
Human Otc DrugPerricone Md Acne Relief Maximum Strength Spot Gel NDC 84448-538
- Generic Name
- Salicylic Acid
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Salicylic Acid
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPerricone Md Acne Relief Calming And Soothing Clay Mask NDC 84448-955
- Generic Name
- Salicylic Acid
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Target Corporation
NDC Product
Human Otc DrugUp And Up Childrens Ibuprofen NDC 11673-593
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugUp And Up Childrens Ibuprofen NDC 11673-741
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Topco Associates LLC
NDC Product
Human Otc DrugTopcare Childrens Ibuprofen NDC 36800-811
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Trigen Laboratories, LLC
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 13811-700
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 13811-706
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 13811-707
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 13811-708
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 13811-709
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 13811-710
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 13811-711
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
U.S. Pharmaceuticals
NDC Product
Human Prescription DrugZavzpret NDC 63539-135
- Generic Name
- Zavegepant
- Dosage Form
- Spray
- Route
- Nasal
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIbrance NDC 63539-284
- Generic Name
- Palbociclib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIbrance NDC 63539-486
- Generic Name
- Palbociclib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIbrance NDC 63539-688
- Generic Name
- Palbociclib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
United Natural Foods, Inc. dba UNFI
NDC Product
Human Otc DrugEqualine Childrens Ibuprofen NDC 41163-710
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Vacation Inc.
NDC Product
Human Otc DrugVacation Spf 50 Super Spritz Face Mist NDC 80641-010
- Generic Name
- Avobenzone, Octisalate, Octocrylene
- Dosage Form
- Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Vertical Pharmaceuticals, LLC
NDC Product
Human Prescription DrugRelexxii NDC 68025-088
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugRelexxii NDC 68025-089
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
WOMENS CHOICE PHARMACEUTICALS LLC
NDC Product
Human Prescription DrugIrospan 24/6 NDC 50967-126
- Generic Name
- Iron, Folic Acid, Vitamin/mineral Supplement
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Wal-Mart Stores Inc
NDC Product
Human Otc DrugEquate Ibuprofen NDC 49035-521
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreen Company
NDC Product
Human Otc DrugChildrens Ibuprofen 100 NDC 0363-1461
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugChildrens Ibuprofen 100 NDC 0363-1521
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
West Coast Paper Company
NDC Product
Human Otc DrugSkin Cleanser NDC 72528-141
- Generic Name
- Chloroxylenol
- Dosage Form
- Soap
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
XLCare Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 72865-133
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 72865-134
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 72865-135
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 72865-136
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
