NDC Product
Human Prescription DrugQuetiapine NDC 16729-145
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Dibasic Calcium Phosphate Dihydrate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) O7TSZ97GEP.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 7789-77-7 and the RxNorm Concept ID (RxCUI) 1311201. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
DIBASIC CALCIUM PHOSPHATE DIHYDRATE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
O7TSZ97GEP
The specific atomic composition represented as a molecular structure string.
InChIKey
Ca.HO4P.2H2O International Chemical Identifier digital signature for unique molecular identification.
SMILES String
XAAHAAMILDNBPS-UHFFFAOYSA-L 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
[Ca+2].OP(=O)([O-])[O-].O.O
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Dibasic Calcium Phosphate Dihydrate. 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
DICALCIUM PHOSPHATE DIHYDRATE
OF
Common Names & Synonyms
CALCII HYDROGENOPHOSPHAS DIHYDRATE [WHO-IP LATIN]
CN
CALCIUM HYDROGEN PHOSPHATE DIHYDRATE [EP MONOGRAPH]
CN
CALCIUM PHOSPHATE DIBASIC, HYDROUS
CN
CALCIUM PHOSPHATE DIHYDRATE [WHO-DD]
CN
CALCIUM PHOSPHATE DIHYDRATE, DIBASIC
CN
CALCIUM PHOSPHATE DIHYDRATE, DIBASIC [USP IMPURITY]
CN
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE
CN
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE [II]
CN
CALCIUM PHOSPHATE, DIBASIC, HYDROUS
CN
CALCIUM PHOSPHATE, DIHYDRATE
CN
CALCIUM PHOSPHATE, DIHYDRATE (1:1)
CN
D.C.P.
CN
DIBASIC CALCIUM PHOSPHATE DIHYDRATE
CN
DIBASIC CALCIUM PHOSPHATE DIHYDRATE [USP MONOGRAPH]
CN
DIBASIC CALCIUM PHOSPHATE HYDRATE
CN
DIBASIC CALCIUM PHOSPHATE HYDRATE [JAN]
CN
PHOSPHORIC ACID, CALCIUM SALT (1:1), DIHYDRATE
CN
Systematic Nomenclature
CALCIUM MONOHYDROGEN PHOSPHATE DIHYDRATE
SYS
CALCIUM PHOSPHATE DIHYDRATE
SYS
NDC Products Containing DIBASIC CALCIUM PHOSPHATE DIHYDRATE
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
Accord Healthcare Inc.
Active Listing
Actavis Pharma, Inc.
NDC Product
Human Prescription DrugLisinopril NDC 0591-0405
- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugLisinopril NDC 0591-0406
- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisinopril NDC 0591-0407
- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugLisinopril NDC 0591-0408
- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisinopril NDC 0591-0409
- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Lisinopril And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugLisinopril And Hydrochlorothiazide NDC 0591-0860
- Generic Name
- Lisinopril And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisinopril And Hydrochlorothiazide NDC 0591-0861
- Generic Name
- Lisinopril And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Lisinopril And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Lisinopril And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugLisinopril And Hydrochlorothiazide NDC 0591-0862
- Generic Name
- Lisinopril And Hydrochlorothiazide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisinopril NDC 0591-0885
- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Lisinopril
- Dosage Form
- Tablet
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Promethazine Hydrochloride
- Dosage Form
- Tablet
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugPromethazine Hydrochloride NDC 0591-5307
- Generic Name
- Promethazine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPromethazine Hydrochloride NDC 0591-5319
- Generic Name
- Promethazine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Allergan, Inc.
NDC Product
Human Prescription DrugSavella NDC 0456-1500
- Generic Name
- Milnacipran Hydrochloride
- Dosage Form
- Kit
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSavella NDC 0456-1510
- Generic Name
- Milnacipran Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSavella NDC 0456-1512
- Generic Name
- Milnacipran Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSavella NDC 0456-1525
- Generic Name
- Milnacipran Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSavella NDC 0456-1550
- Generic Name
- Milnacipran Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Aurolife Pharma LLC
NDC Product
Human Prescription DrugGlycopyrrolate NDC 13107-014
- Generic Name
- Glycopyrrolate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 13107-154
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 13107-155
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 13107-156
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 13107-157
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bayer HealthCare LLC.
NDC Product
Human Otc DrugMidol Bloat Relief NDC 0280-0070
- Generic Name
- Pamabrom
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugClaritin-d 24 Hour NDC 11523-4332
- Generic Name
- Loratadine And Pseudoephedrine Sulfate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Bell Pharmaceuticals, Inc.
NDC Product
Human Otc DrugJet-asleep Double Strength Night Time Sleep Aid NDC 15579-828
- Generic Name
- Diphenhydramine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Endo USA, Inc.
NDC Product
Human Prescription DrugBenztropine Mesylate NDC 0603-2433
- Generic Name
- Benztropine Mesylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBenztropine Mesylate NDC 0603-2434
- Generic Name
- Benztropine Mesylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBenztropine Mesylate NDC 0603-2435
- Generic Name
- Benztropine Mesylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA Inc
NDC Product
Human Prescription DrugPyrazinamide NDC 0054-0812
- Generic Name
- Pyrazinamide
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Suphedrine 12 Hour NDC 0113-0054
- Generic Name
- Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nighttime Sleep Aid NDC 0113-0431
- Generic Name
- Diphenhydramine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Nasal Decongestant NDC 0113-0432
- Generic Name
- Pseudoephedrine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Sleep Aid NDC 0113-0441
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Allergy Relief NDC 0113-0479
- Generic Name
- Diphenhydramine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSinus 12 Hour NDC 0113-2017
- Generic Name
- Pseudoephedrine Hcl
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
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
NDC Product
Human Otc DrugGood Sense Sleep Aid Ultra NDC 0113-6044
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lannett Company, Inc.
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 0527-0586
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 0527-1282
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 0527-1788
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 0527-1789
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 0527-1790
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 0527-1791
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Major Pharmaceuticals
NDC Product
Human Otc DrugSleep Tabs NDC 0904-4274
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSudogest NDC 0904-5053
- Generic Name
- Pseudoephedrine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSudogest Nasal Decongestant NDC 0904-6337
- Generic Name
- Pseudoephedrine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugQuetiapine NDC 0904-6638
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine NDC 0904-6639
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine NDC 0904-6640
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine NDC 0904-6641
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine NDC 0904-6642
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine NDC 0904-6643
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugHaloperidol NDC 0904-6661
- Generic Name
- Haloperidol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGlycopyrrolate NDC 0904-6709
- Generic Name
- Glycopyrrolate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSudogest 12 Hour NDC 0904-6754
- Generic Name
- Pseudoephedrine Hcl
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 0904-6988
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 0904-7157
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 0904-7158
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 0904-7159
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 0904-7160
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSennosides NDC 0904-7252
- Generic Name
- Sennosides
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugBenztropine Mesylate NDC 0904-7288
- Generic Name
- Benztropine Mesylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBenztropine Mesylate NDC 0904-7289
- Generic Name
- Benztropine Mesylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBenztropine Mesylate NDC 0904-7290
- Generic Name
- Benztropine Mesylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSennosides, Docusate Sodium NDC 0904-7440
- Generic Name
- Sennosides, Docusate Sodium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugBaclofen NDC 0904-7552
- Generic Name
- Baclofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBaclofen NDC 0904-7553
- Generic Name
- Baclofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Marlex Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 10135-725
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 10135-726
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 10135-727
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochloride NDC 10135-728
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugTicagrelor NDC 0378-2214
- Generic Name
- Ticagrelor
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTicagrelor NDC 0378-2215
- Generic Name
- Ticagrelor
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 0378-7001
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 0378-7002
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 0378-7003
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 0378-7004
- Generic Name
- Paroxetine Hydrochloride Hemihydrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNorethindrone And Ethinyl Estradiol And Ferrous Fumarate NDC 0378-7297
- Generic Name
- Norethindrone And Ethinyl Estradiol And Ferrous Fumarate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugBenztropine Mesylate NDC 0615-8222
- Generic Name
- Benztropine Mesylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSenexon-s NDC 0615-8331
- Generic Name
- Docusate Sodium 50mg And Sennosides 8.6mg
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 0615-8359
- Generic Name
- Paroxetine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSenna Time NDC 0615-8402
- Generic Name
- Sennosides
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugHydroxychloroquine Sulfate NDC 0615-8459
- Generic Name
- Hydroxychloroquine Sulfate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 0615-8470
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 0615-8471
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 0615-8472
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 0615-8473
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 0615-8474
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBenztropine Mesylate NDC 0615-8478
- Generic Name
- Benztropine Mesylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBaclofen NDC 0615-8518
- Generic Name
- Baclofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGlycopyrrolate NDC 0615-8617
- Generic Name
- Glycopyrrolate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NorthStar Rx LLC
NDC Product
Human Prescription DrugParoxetine NDC 16714-181
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 16714-182
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 16714-183
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugParoxetine NDC 16714-184
- Generic Name
- Paroxetine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 16714-375
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 16714-376
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 16714-377
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 16714-378
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 16714-379
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 16714-380
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 16714-611
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 16714-612
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 16714-613
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Northstar Rx LLC.
NDC Product
Human Prescription DrugHydroxychloroquine Sulfate NDC 16714-110
- Generic Name
- Hydroxychloroquine Sulfate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Pharbest Pharmaceuticals, Inc.
NDC Product
Human Otc DrugSenna-s NDC 16103-378
- Generic Name
- Sennosides 8.6mg And Docusate Sodium 50mg
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
RUGBY LABORATORIES
NDC Product
Human Otc DrugSenexon-s NDC 0536-1247
- Generic Name
- Docusate Sodium 50mg And Sennosides 8.6mg
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugStimulant Laxative Plus Stool Softener NDC 0536-1248
- Generic Name
- Docusate Sodium 50 Mg And Sennosides 8.6 Mg
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rising Pharma Holdings, Inc.
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 16571-126
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 16571-127
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 16571-717
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 16571-718
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 16571-719
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 16571-720
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 16571-721
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 16571-722
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDarifenacin NDC 16571-767
- Generic Name
- Darifenacin
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDarifenacin NDC 16571-768
- Generic Name
- Darifenacin
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine Fumarate NDC 16571-809
- Generic Name
- Quetiapine Fumarate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochoride NDC 16571-889
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochoride NDC 16571-890
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochoride NDC 16571-891
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluphenazine Hydrochoride NDC 16571-892
- Generic Name
- Fluphenazine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rite Aid Corporation
NDC Product
Human Otc DrugSenna NDC 11822-0298
- Generic Name
- Sennosides
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAllergy Relief NDC 11822-0329
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSleep Aid NDC 11822-0441
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSinus Pressure And Congestion Relief Maximum Strength NDC 11822-0650
- Generic Name
- Pseudoephedrine Hcl
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSleep Aid NDC 11822-0672
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLaxative NDC 11822-0773
- Generic Name
- Sennosides
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugStay Awake NDC 11822-2260
- Generic Name
- Caffeine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSleep Aid NDC 11822-3000
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSinus Pressure And Congestion Relief NDC 11822-9485
- Generic Name
- Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rugby Laboratories
NDC Product
Human Otc DrugDiphenhydramine Hcl NDC 0536-1214
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Sheffield Pharmaceuticals LLC
NDC Product
Human Otc DrugDr. Sheffield Sensitive Care NDC 11527-420
- Generic Name
- Sensitive Tooth Paste
- Dosage Form
- Paste, Dentifrice
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
SpecGx LLC
NDC Product
Human Prescription DrugMethadose Dispersible NDC 0406-0540
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethadone Hydrochloride NDC 0406-2540
- Generic Name
- Methadone Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
TARGET CORPORATION
NDC Product
Human Otc DrugSenna Laxative NDC 11673-191
- Generic Name
- Sennosides 8.6 Mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugStool Softening Senna Laxative NDC 11673-192
- Generic Name
- Sennosides 8.6 Mg - Docusate Sodium 50 Mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH NOT FINAL
Active Listing
NDC Product
Human Otc DrugStool Softener And Stimulant Laxative NDC 11673-209
- Generic Name
- Docusate Sodium And Sennosides
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAllergy Relief NDC 11673-494
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNighttime Sleep Aid NDC 11673-496
- Generic Name
- Diphenydramine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMaximum Strength Laxative Pills NDC 11673-995
- Generic Name
- Sennosides
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Target Corporation
NDC Product
Human Otc DrugUp And Up Nighttime Sleep Aid NDC 11673-171
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugQuetiapine NDC 0093-2063
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBisoprolol Fumarate And Hydrochlorothiazide NDC 0093-3242
- Generic Name
- Bisoprolol Fumarate And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Bisoprolol Fumarate And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Bisoprolol Fumarate And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugBisoprolol Fumarate And Hydrochlorothiazide NDC 0093-3243
- Generic Name
- Bisoprolol Fumarate And Hydrochlorothiazide
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugQuetiapine NDC 0093-8162
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine NDC 0093-8163
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine NDC 0093-8164
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine NDC 0093-8165
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugQuetiapine NDC 0093-8166
- Generic Name
- Quetiapine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBaclofen NDC 0172-4096
- Generic Name
- Baclofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBaclofen NDC 0172-4097
- Generic Name
- Baclofen
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMegestrol Acetate NDC 0555-0606
- Generic Name
- Megestrol Acetate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMegestrol Acetate NDC 0555-0607
- Generic Name
- Megestrol Acetate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEstradiol NDC 0555-0886
- Generic Name
- Estradiol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEstradiol NDC 0555-0887
- Generic Name
- Estradiol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEstradiol NDC 0555-0899
- Generic Name
- Estradiol
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBalziva NDC 0555-9034
- Generic Name
- Norethindrone And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
WALGREENS
NDC Product
Human Otc DrugAllergy Relief NDC 0363-0100
- Generic Name
- Diphenhydramine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLaxative NDC 0363-9978
- Generic Name
- Sennosides
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreen Company
NDC Product
Human Otc DrugSleep Ii Nighttime Sleep Aid NDC 0363-0189
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSleep Aid Nighttime NDC 0363-0367
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAnti-diarrheal NDC 0363-0375
- Generic Name
- Loperamide Hcl
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSleep Aid NDC 0363-0386
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNasal Decongestant D NDC 0363-1214
- Generic Name
- Pseudoephedrine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAllergy Relief NDC 0363-1799
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMotion Sickness Relief NDC 0363-1980
- Generic Name
- Dimenhydrinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAllergy Relief NDC 0363-3291
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugNasal Decongestant D NDC 0363-3301
- Generic Name
- Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- 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 DrugNasal Decongestant Pe NDC 0363-4531
- Generic Name
- Phenylephrine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSinus Pe Congestion NDC 0363-4534
- Generic Name
- Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAllergy Relief Plus Congestion NDC 0363-4851
- Generic Name
- Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCaffeine NDC 0363-5009
- Generic Name
- Caffeine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEphedrine Sulfate NDC 0363-5789
- Generic Name
- Ephedrine Sulfate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAllergy Relief NDC 0363-6141
- Generic Name
- Diphenhydramine Hcl
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
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
NDC Product
Human Otc DrugUltra Sleep Aid NDC 0363-8011
- Generic Name
- Doxylamine Succinate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreens
NDC Product
Human Otc DrugSenna Laxative NDC 0363-0138
- Generic Name
- Sennosides
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugStool Softener Laxative Plus Stimulant NDC 0363-0827
- Generic Name
- Docusate Sodium And Sennosides
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSenna S NDC 0363-0883
- Generic Name
- Docusate Sodium, Sennosides
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugStool Softener Laxative NDC 0363-8550
- Generic Name
- Docusate Sodium And Sennosides
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSenna NDC 0363-8820
- Generic Name
- Sennosides
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
walgreens
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
