NDC Product
Human Prescription DrugKaletra NDC 0074-0522
- Generic Name
- Lopinavir And Ritonavir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Copovidone K25-31, uniquely identified by the FDA Unique Ingredient Identifier (UNII) D9C330MD8B.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 25086-89-9 and the RxNorm Concept ID (RxCUI) N/A. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
FDA UNII Code
D9C330MD8B
CAS Registry Number
25086-89-9
RxNorm Concept ID
N/A
Detailed Substance Profile
Preferred Name
COPOVIDONE K25-31
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
D9C330MD8B
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
Substance Type
polymer
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Copovidone K25-31. 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
VP/VA COPOLYMER
OF
Common Names & Synonyms
COPOLYMER OF 1-VINYL-2-PYRROLIDONE AND VINYL ACETATE IN THE MASS PROPORTION OF 3:2 (MW=40000)
CN
COPOVIDONE
CN
COPOVIDONE (PLASDONE-S630)
CN
COPOVIDONE [EP IMPURITY]
CN
COPOVIDONE [EP MONOGRAPH]
CN
COPOVIDONE [FCC]
CN
COPOVIDONE [MART.]
CN
COPOVIDONE [USP-RS]
CN
COPOVIDONE [WHO-DD]
CN
COPOVIDONE K25-31
CN
COPOVIDONE K26-29
CN
COPOVIDONE K28
CN
PLASDONE-S630
CN
POLYVINYLPYRROLIDONE/VINYL ACETATE COPOLYMER
CN
POVIDONE/VINYL ACETATE COPOLYMER
CN
PVP/VA COPOLYMER
CN
Brand / Trade Names
KOLLIDON VA 64
BN
Technical Codes
NSC-114023
CD
NSC-114024
CD
NSC-114025
CD
NSC-114026
CD
NDC Products Containing COPOVIDONE K25-31
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 DrugVenclexta NDC 0074-0561
- Generic Name
- Venetoclax
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugVenclexta NDC 0074-0566
- Generic Name
- Venetoclax
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugVenclexta NDC 0074-0576
- Generic Name
- Venetoclax
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugVenclexta NDC 0074-0579
- Generic Name
- Venetoclax
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
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 DrugMavyret NDC 0074-2600
- Generic Name
- Glecaprevir And Pibrentasvir
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugMavyret NDC 0074-2625
- Generic Name
- Glecaprevir And Pibrentasvir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNorvir NDC 0074-3399
- Generic Name
- Ritonavir
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugKaletra NDC 0074-3956
- Generic Name
- Lopinavir And Ritonavir
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugKaletra NDC 0074-6799
- Generic Name
- Lopinavir And Ritonavir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugQulipta NDC 0074-7094
- Generic Name
- Atogepant
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugQulipta NDC 0074-7095
- Generic Name
- Atogepant
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugQulipta NDC 0074-7096
- Generic Name
- Atogepant
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Accord Healthcare Inc.
NDC Product
Human Prescription DrugPirfenidone NDC 16729-467
- Generic Name
- Pirfenidone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPirfenidone NDC 16729-468
- Generic Name
- Pirfenidone
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Actavis Pharma, Inc.
NDC Product
Human Prescription DrugLamotrigine NDC 0228-1638
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMesalamine NDC 0591-2245
- Generic Name
- Mesalamine
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTranexamic Acid NDC 0591-3720
- Generic Name
- Tranexamic Acid
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alembic Labs LLC
NDC Product
Human Prescription DrugGlycopyrrolate NDC 15955-305
- Generic Name
- Glycopyrrolate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGlycopyrrolate NDC 15955-318
- Generic Name
- Glycopyrrolate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetronidazole NDC 15955-388
- Generic Name
- Metronidazole
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetronidazole NDC 15955-389
- Generic Name
- Metronidazole
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Allergan, Inc.
NDC Product
Human Prescription DrugCelexa NDC 0456-4010
- Generic Name
- Citalopram
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCelexa NDC 0456-4020
- Generic Name
- Citalopram
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCelexa NDC 0456-4040
- Generic Name
- Citalopram
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
AmerisourceBergen Drug Corp
NDC Product
Human Otc DrugGood Neighbor Pharmacy Mucus Relief NDC 24385-602
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Amneal Pharmaceuticals of New York LLC
NDC Product
Human Prescription DrugColesevelam Hydrochloride NDC 0115-1320
- Generic Name
- Colesevelam Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugColestipol Hydrochloride NDC 0115-5211
- Generic Name
- Colestipol Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 0115-8211
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
AstraZeneca Pharmaceuticals LP
NDC Product
Human Prescription DrugLynparza NDC 0310-0668
- Generic Name
- Olaparib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLynparza NDC 0310-0679
- Generic Name
- Olaparib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCalquence NDC 0310-3512
- Generic Name
- Acalabrutinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTruqap NDC 0310-9500
- Generic Name
- Capivasertib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTruqap NDC 0310-9501
- Generic Name
- Capivasertib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Aurolife Pharma, LLC
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 13107-380
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 13107-381
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 13107-382
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvKARE
NDC Product
Human Prescription DrugRamelteon NDC 42291-776
- Generic Name
- Ramelteon
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugUrsodiol NDC 42291-931
- Generic Name
- Ursodiol
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 42291-989
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bayer HealthCare LLC.
NDC Product
Human Otc DrugAlka-seltzer Cool Action Heartburn Relief Mint NDC 0280-0001
- Generic Name
- Calcium Carbonate
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAlka-seltzer Heartburn Relief Peppermint NDC 0280-0002
- Generic Name
- Calcium Carbonate
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Better Living Brands, LLC
NDC Product
Human Otc DrugChildrens Pain Relief NDC 21130-223
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Burel Pharmaceuticals, LLC
NDC Product
Human Prescription DrugTadalafil NDC 35573-460
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 35573-461
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 35573-462
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 35573-463
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Calvin Scott & Co., Inc.
NDC Product
Human Prescription DrugMetformin Hydrochloride Extended-release 500mg NDC 17224-311
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugGabapentin NDC 31722-091
- Generic Name
- Gabapentin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGabapentin NDC 31722-092
- Generic Name
- Gabapentin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLopinavir And Ritonavir NDC 31722-556
- Generic Name
- Lopinavir And Ritonavir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRitonavir NDC 31722-597
- Generic Name
- Ritonavir
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLopinavir And Ritonavir NDC 31722-603
- Generic Name
- Lopinavir And Ritonavir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 31722-643
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 31722-644
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 31722-645
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 31722-646
- Generic Name
- Tadalafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTadalafil NDC 31722-647
- Generic Name
- Tadalafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMoxifloxacin NDC 31722-845
- Generic Name
- Moxifloxacin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Chattem, Inc.
NDC Product
Human Otc DrugAllegra-d Allergy And Congestion NDC 41167-4320
- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Eli Lilly and Company
NDC Product
Human Prescription DrugFoundayo NDC 0002-4178
- Generic Name
- Orforglipron
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFoundayo NDC 0002-4503
- Generic Name
- Orforglipron
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFoundayo NDC 0002-4794
- Generic Name
- Orforglipron
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFoundayo NDC 0002-4803
- Generic Name
- Orforglipron
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFoundayo NDC 0002-4839
- Generic Name
- Orforglipron
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFoundayo NDC 0002-4953
- Generic Name
- Orforglipron
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Endo USA, Inc.
NDC Product
Human Prescription DrugPenicillamine NDC 0254-2000
- Generic Name
- Penicillamine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Gensco Laboratories LLC
NDC Product
Human Prescription DrugRizafilm NDC 35781-0600
- Generic Name
- Rizatriptan Benzoate
- Dosage Form
- Film
- Route
- Oral
- Marketing
- NDA
Active Listing
H E B
NDC Product
Human Otc DrugMucus Relief Dm NDC 37808-812
- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
HEB
NDC Product
Human Otc DrugPain Relief Pm Extra Strength NDC 37808-795
- Generic Name
- Acetaminophen And Diphenhydramine Hydrochloride
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
HYVEE INC
NDC Product
Human Otc DrugPain Relief Pm NDC 42507-095
- Generic Name
- Acetaminophen And Diphenhydramine Hydrochloride
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAdvil NDC 0573-0133
- Generic Name
- Ibuprofen Sodium
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAdvil NDC 0573-0134
- Generic Name
- Ibuprofen Sodium
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAdvil Menstrual Pain NDC 0573-0230
- Generic Name
- Ibuprofen Sodium
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
HyVee Inc
NDC Product
Human Otc DrugMucus Dm NDC 42507-222
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMucus Er NDC 42507-471
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Multilayer, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMucus Dm NDC 42507-812
- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
KROGER COMPANY
NDC Product
Human Otc DrugMucus Relief NDC 41226-723
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMaximum Strength Mucus Relief NDC 41226-724
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Kroger Company
NDC Product
Human Otc DrugLansoprazole NDC 30142-192
- Generic Name
- Lansoprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
L Perrigo Company
NDC Product
Human Otc DrugGood Sense Mucus Dm NDC 0113-0812
- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Lansoprazole NDC 0113-0116
- Generic Name
- Lansoprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugGood Sense Mucus Dm NDC 0113-2219
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Mucus Er NDC 0113-4077
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Multilayer, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Laurus Labs Limited
NDC Product
Human Prescription DrugLopinavir And Ritonavir NDC 42385-933
- Generic Name
- Lopinavir And Ritonavir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLopinavir And Ritonavir NDC 42385-934
- Generic Name
- Lopinavir And Ritonavir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
MARKSANS PHARMA LIMITED
NDC Product
Human Otc DrugGuaifenesin 1200 Mg NDC 25000-041
- Generic Name
- Guaifenesin 1200 Mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin 600 Mg NDC 25000-042
- Generic Name
- Guaifenesin 600 Mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Macleods Pharmaceuticals Limited
NDC Product
Human Prescription DrugLopinavir And Ritonavir NDC 33342-163
- Generic Name
- Lopinavir And Ritonavir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLopinavir And Ritonavir NDC 33342-164
- Generic Name
- Lopinavir And Ritonavir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Major Pharmaceuticals
NDC Product
Human Prescription DrugIbuprofen NDC 0904-5853
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIbuprofen NDC 0904-5854
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIbuprofen NDC 0904-5855
- Generic Name
- Ibuprofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCitalopram NDC 0904-6084
- Generic Name
- Citalopram
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCitalopram NDC 0904-6085
- Generic Name
- Citalopram
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLinezolid NDC 0904-6553
- Generic Name
- Linezolid
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGabapentin NDC 0904-6823
- Generic Name
- Gabapentin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetaxalone NDC 0904-6831
- Generic Name
- Metaxalone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugUrsodiol NDC 0904-6890
- Generic Name
- Ursodiol
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Meijer Distribution Inc
NDC Product
Human Otc DrugMucus Relief Dm NDC 41250-436
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMucus Dm NDC 41250-812
- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMeijer Pain Relief Patches NDC 41250-972
- Generic Name
- Lidocaine
- Dosage Form
- Patch
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Meijer Distribution Inc.
NDC Product
Human Otc DrugMeijer Chest Congestion Relief NDC 41250-713
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugBelsomra NDC 0006-0005
- Generic Name
- Suvorexant
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBelsomra NDC 0006-0033
- Generic Name
- Suvorexant
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBelsomra NDC 0006-0325
- Generic Name
- Suvorexant
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBelsomra NDC 0006-0335
- Generic Name
- Suvorexant
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZepatier NDC 0006-3074
- Generic Name
- Elbasvir And Grazoprevir
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Micro Labs Limited
NDC Product
Human Prescription DrugRamelteon NDC 42571-375
- Generic Name
- Ramelteon
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Misemer Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugMetaxalone NDC 0276-0508
- Generic Name
- Metaxalone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugScopolamine NDC 0378-6470
- Generic Name
- Scopolamine
- Dosage Form
- Patch
- Route
- Transdermal
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRivastigmine NDC 0378-9070
- Generic Name
- Rivastigmine
- Dosage Form
- Patch
- Route
- Transdermal
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRivastigmine NDC 0378-9071
- Generic Name
- Rivastigmine
- Dosage Form
- Patch
- Route
- Transdermal
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRivastigmine NDC 0378-9072
- Generic Name
- Rivastigmine
- Dosage Form
- Patch
- Route
- Transdermal
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugCitalopram NDC 0615-8022
- Generic Name
- Citalopram Hydrobromide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCitalopram NDC 0615-8023
- Generic Name
- Citalopram Hydrobromide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCitalopram NDC 0615-8141
- Generic Name
- Citalopram Hydrobromide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NorthStar Rx LLC
NDC Product
Human Prescription DrugGabapentin NDC 16714-330
- Generic Name
- Gabapentin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGabapentin NDC 16714-332
- Generic Name
- Gabapentin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Novartis Pharmaceuticals Corporation
NDC Product
Human Prescription DrugRhapsido NDC 0078-1483
- Generic Name
- Remibrutinib
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugXeljanz Xr NDC 0069-0501
- Generic Name
- Tofacitinib
- Dosage Form
- Tablet, Film Coated, Extended Release
- 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 0069-1002
- Generic Name
- Tofacitinib
- Dosage Form
- Tablet, Film Coated
- 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
NDC Product
Human Prescription DrugPaxlovid NDC 0069-5045
- Generic Name
- Nirmatrelvir And Ritonavir
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPaxlovid NDC 0069-5317
- Generic Name
- Nirmatrelvir And Ritonavir
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPaxlovid NDC 0069-5321
- Generic Name
- Nirmatrelvir And Ritonavir
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
QPharma, Inc.
NDC Product
Human Prescription DrugCitalopram NDC 42708-019
- Generic Name
- Citalopram Hydrobromide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Reese Pharmaceutical Co
NDC Product
Human Otc DrugDg Health Immediate Release Mucus Relief NDC 10956-059
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rising Pharma Holdings, Inc.
NDC Product
Human Prescription DrugGabapentin NDC 16571-117
- Generic Name
- Gabapentin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGabapentin NDC 16571-226
- Generic Name
- Gabapentin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rite Aid Corporation
NDC Product
Human Otc DrugMucus Relief Dm Max NDC 11822-1812
- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMucus Relief Dm NDC 11822-2219
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rugby Laboratories
NDC Product
Human Otc DrugMucus Relief Er NDC 0536-1249
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Chest Congestion Relief G450 NDC 0536-1311
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRugby Mucus Relief Dm Er NDC 0536-1446
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Mucus Relief Dm Er NDC 0536-1447
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Mucus Relief Er NDC 0536-1451
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Multilayer, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Safeway
NDC Product
Human Otc DrugPain Relief Pm NDC 21130-095
- Generic Name
- Acetaminophen And Diphenhydramine Hydrochloride
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Sigmapharm Laboratories, LLC
NDC Product
Human Prescription DrugAdefovir Dipivoxil NDC 42794-003
- Generic Name
- Adefovir Dipivoxil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAsenapine NDC 42794-016
- Generic Name
- Asenapine
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAsenapine NDC 42794-017
- Generic Name
- Asenapine
- Dosage Form
- Tablet
- Route
- Sublingual
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDofetilide NDC 42794-044
- Generic Name
- Dofetilide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDofetilide NDC 42794-045
- Generic Name
- Dofetilide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDofetilide NDC 42794-046
- Generic Name
- Dofetilide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
TOPCO ASSOCIATES LLC
NDC Product
Human Otc DrugTopcare Chest Congestion Relief NDC 36800-794
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTopcare Chest Congestion And Cough Relief Dm NDC 36800-988
- Generic Name
- Dextromethorphan Hydrobromide / Guaifenesin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
TRP Company
NDC Product
Human Otc DrugAsthma Therapy NDC 17312-017
- Generic Name
- Arsenic Trioxide - Histamine Dihydrochloride - Dermatophagoi...
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugBronchial Cough Therapy NDC 17312-018
- Generic Name
- Antimony Potassium Tartrate - Protortonia Cacti - Drosera Ro...
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugIrritable Bowel Syndrome Therapy NDC 17312-019
- Generic Name
- Asafetida - Bismuth Subnitrate - Bryonia Alba Root - Activat...
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugSciatica Therapy NDC 17312-021
- Generic Name
- Arnica Montana - Citrullus Colocynthis Fruit Pulp - Pseudogn...
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugRing Relief NDC 17312-023
- Generic Name
- Arnica Montana - Calcium Sulfide - Hypericum Perforatum - Ly...
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugEarache Relief NDC 17312-025
- Generic Name
- Apis Mellifera, Arnica Montana, Atropa Belladonna, Tribasic ...
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugHeartburn Relief NDC 17312-030
- Generic Name
- Carbo More
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugConstipation Relief NDC 17312-031
- Generic Name
- Aloe, Potassium Alum, Oyster Shell Calcium Carbonate, Crude ...
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugMigraine Headache Therapy NDC 17312-041
- Generic Name
- Atropa Belladonna - Bryonia Alba Root - Black Cohosh - Arabi...
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugChronic Fatigue Therapy NDC 17312-170
- Generic Name
- Epinephrine, Gold, Chelidonium Majus, Echinacea, Ginkgo, Hel...
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugFibromyalgia Relief NDC 17312-171
- Generic Name
- Bryonia Alba Root - Causticum - Loeselia Mexicana Whole - Ma...
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugCom-pare2 Flu Relief NDC 17312-179
- Generic Name
- Anas Barbariae
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugNatural Relief Arthritis Therapy NDC 17312-437
- Generic Name
- Apis Mellifera, Salicylic Acid, Ruta Graveolens, Toxicodendr...
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugNatural Relief Diarrhea Relief NDC 17312-473
- Generic Name
- Aloe, Citrullus Colocynthis, Croton Tiglium, Lycopodium Clav...
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugNatural Eyes Floaters Relief NDC 17312-478
- Generic Name
- Chelidonium, Euphrasia, Kali Sulph, Natrum Muriaticum, Phosp...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Target Corporation
NDC Product
Human Otc DrugUp And Up Mucus Relief Dm NDC 11673-716
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugMimvey NDC 0093-5455
- Generic Name
- Estradiol And Norethindrone Acetate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugPhentermine And Topiramate NDC 0480-2299
- Generic Name
- Phentermine And Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Phentermine And Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugAlvaiz NDC 0480-3273
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAlvaiz NDC 0480-3274
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAlvaiz NDC 0480-3275
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAlvaiz NDC 0480-3276
- Generic Name
- Eltrombopag
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Phentermine And Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugPhentermine And Topiramate NDC 0480-3295
- Generic Name
- Phentermine And Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhentermine And Topiramate NDC 0480-3296
- Generic Name
- Phentermine And Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Phentermine And Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Phentermine And Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugPhentermine And Topiramate NDC 0480-3297
- Generic Name
- Phentermine And Topiramate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
TopCo Associates LLC
NDC Product
Human Otc DrugPain Relief Pm Extra Strength NDC 36800-095
- Generic Name
- Acetaminophen And Diphenhydramine Hydrochloride
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Topco Associates LLC
NDC Product
Human Otc DrugTopcare Mucus Dm NDC 36800-219
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugTopcare Lansoprazole NDC 36800-295
- Generic Name
- Lansoprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugTopcare Mucus Dm NDC 36800-592
- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Torrent Pharmaceuticals Limited
NDC Product
Human Prescription DrugLevetiracetam NDC 13668-272
- Generic Name
- Levetiracetam
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevetiracetam NDC 13668-300
- Generic Name
- Levetiracetam
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Unichem Pharmaceuticals (USA), Inc.
NDC Product
Human Prescription DrugBisoprolol Fumarate And Hydrochlorothiazide NDC 29300-187
- Generic Name
- Bisoprolol Fumarate And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBisoprolol Fumarate And Hydrochlorothiazide NDC 29300-188
- Generic Name
- Bisoprolol Fumarate And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBisoprolol Fumarate And Hydrochlorothiazide NDC 29300-189
- Generic Name
- Bisoprolol Fumarate And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
United Natural Foods, Inc. dba UNFI
NDC Product
Human Otc DrugEqualine Chest Congestion Relief NDC 41163-113
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAcetaminophen Pm Extra Strength NDC 41163-515
- Generic Name
- Acetaminophen And Diphenhydramine Hydrochloride
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEqualine Mucus Dm NDC 41163-599
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugEqualine Mucus Dm NDC 41163-781
- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREEN CO.
NDC Product
Human Otc DrugAcetaminophen NDC 0363-9605
- Generic Name
- Acetaminophen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreen Company
NDC Product
Human Otc DrugLansoprazole NDC 0363-1419
- Generic Name
- Lansoprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugMucus Relief Dm NDC 0363-3219
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMucus Relief Dm NDC 0363-6812
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugLeg Cramps Pm NDC 0363-7174
- Generic Name
- Oyster Shell Calcium Carbonate, Crude, Causticum, Matricaria...
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugPain Relief Patches NDC 0363-9110
- Generic Name
- Lidocaine
- Dosage Form
- Patch
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPain Relief Patches NDC 0363-9116
- Generic Name
- Lidocaine
- Dosage Form
- Kit
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
