NDC Product
Human Otc Drug- Generic Name
- Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Vanillin, uniquely identified by the FDA Unique Ingredient Identifier (UNII) CHI530446X.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 121-33-5 and the RxNorm Concept ID (RxCUI) 1368176. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
VANILLIN
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
CHI530446X
The specific atomic composition represented as a molecular structure string.
InChIKey
C8H8O3 International Chemical Identifier digital signature for unique molecular identification.
SMILES String
MWOOGOJBHIARFG-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
c1(c(ccc(c1)C=O)O)OC
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Vanillin. 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
VANILLIN
OF
Common Names & Synonyms
4-HYDROXY-3-METHOXY-BENZYLDEHYDE
CN
METHYLPROTOCATECHUIC ALDEHYDE
CN
P-HYDROXY-M-METHOXYBENZALDEHYDE
CN
RHOVANIL
CN
VANILLIC ALDEHYDE
CN
VANILLIN [EP MONOGRAPH]
CN
VANILLIN [FCC]
CN
VANILLIN [FHFI]
CN
VANILLIN [HSDB]
CN
VANILLIN [II]
CN
VANILLIN [MART.]
CN
VANILLIN [MI]
CN
VANILLIN [USP-RS]
CN
VANILLIN [VANDF]
CN
VANILLIN [WHO-DD]
CN
VANILLIN MELTING POINT STANDARD
CN
VANILLIN, NATURAL [FHFI]
CN
Brand / Trade Names
LIOXIN
BN
Systematic Nomenclature
3-METHOXY-4-HYDROXYBENZALDEHYDE
SYS
4-HYDROXY-3-METHOXYBENZALDEHYDE
SYS
4-HYDROXY-M-ANISALDEHYDE
SYS
BENZALDEHYDE, 4-HYDROXY-3-METHOXY-
SYS
VANILLALDEHYDE
SYS
Technical Codes
FEMA NO. 3107
CD
H-0264
CD
NPLC-0145
CD
NSC-15351
CD
NSC-403658
CD
NSC-48383
CD
NDC Products Containing VANILLIN
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 (426), only Active Listings are currently displayed. Display is limited to the first 200 products.
Showing 200 active products
9055-7588 Quebec Inc. DBA Attitude
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Ethyl Alcohol
- Dosage Form
- Solution
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
9055-7588 Qu�bec Inc. DBA Attitude
NDC Product
Human Otc DrugAttitude - Leaves Bar - Lip Balm - Spf 15 - Mango NDC 61649-983
- Generic Name
- Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
9055-7588 Qu�bec Inc.DBA ATTITUDE
NDC Product
Human Otc Drug- Generic Name
- Zinc Oxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Zinc Oxide
- Dosage Form
- Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAttitude Sunly Lip Balm Spf 15 Coconut NDC 61649-553
- Generic Name
- Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAttitude Sunly Lip Balm Spf 15 Pineapple NDC 61649-555
- Generic Name
- Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAttitude Sunly Lip Balm Spf 15 Watermelon NDC 61649-557
- Generic Name
- Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAttitude Super Leaves Lip Balm Spf 15 Coconut NDC 61649-923
- Generic Name
- Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAttitude Super Leaves Lip Balm Spf 15 Exotic NDC 61649-925
- Generic Name
- Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAttitude Super Leaves Lip Balm Spf 15 Watermelon NDC 61649-927
- Generic Name
- Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
A-S Medication Solutions
NDC Product
Human Prescription DrugClarithromycin NDC 50090-0927
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClarithromycin NDC 50090-1830
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 50090-2007
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 50090-3574
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 50090-4861
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 50090-7121
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline NDC 50090-7230
- Generic Name
- Sertraline
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline NDC 50090-7295
- Generic Name
- Sertraline
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 50090-7661
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 50090-7662
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 50090-7698
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 50090-7699
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 50090-7700
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 50090-7701
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 50090-7830
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alembic Pharmaceuticals Inc.
NDC Product
Human Prescription DrugClarithromycin NDC 62332-344
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClarithromycin NDC 62332-345
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alembic Pharmaceuticals Limited
NDC Product
Human Prescription DrugClarithromycin NDC 46708-344
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClarithromycin NDC 46708-345
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alliance Pharma Inc.
NDC Product
Human Otc DrugVamousse Lice Treatment NDC 72238-001
- Generic Name
- Pediculicide
- Dosage Form
- Aerosol, Foam
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugVamousse Lice Treatment Complete Kit NDC 72238-003
- Generic Name
- Sodium Chloride And Eucalyptus Globulus Leaf
- Dosage Form
- Kit
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugVamousse Pro Total Lice Emergency Kit NDC 72238-005
- Generic Name
- Pediculicide
- Dosage Form
- Kit
- Route
- Topical
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Allure Labs
NDC Product
Human Otc Drug3d Tinted Moisturizing Bs Spf 30 NDC 62742-4277
- Generic Name
- Zinc Oxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Allure Labs, Inc
NDC Product
Human Otc DrugMineral Sunscreen Broad Spectrum Spf 45 NDC 62742-4152
- Generic Name
- Zinc Oxide And Titanium Dioxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH FINAL
Active Listing
NDC Product
Human Otc DrugMineral Sunscreen Moisturizer Broad Spectrum Spf 20 NDC 62742-4153
- Generic Name
- Zinc Oxide And Titanium Dioxide
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH FINAL
Active Listing
American Health Packaging
NDC Product
Human Prescription DrugMesalamine NDC 60687-650
- Generic Name
- Mesalamine
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 60687-857
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 60687-868
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 60687-879
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClarithromycin NDC 68002-104
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 68084-776
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 68084-782
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Andalou naturals
NDC Product
Human Otc Drug1000 Roses Daily Shade Facial Spf 18 NDC 55560-0103
- Generic Name
- Octisalate, Octocrylene, And Avobenzone
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug1000 Roses Cc Color Plus Correct Sheer Tan Spf 30 NDC 55560-0106
- Generic Name
- Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Aphena Pharma Solutions - Tennessee, LLC
NDC Product
Human Prescription DrugDivalproex Sodium NDC 71610-031
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 71610-032
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Ascend Laboratories, LLC
NDC Product
Human Prescription DrugMesalamine NDC 67877-717
- Generic Name
- Mesalamine
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Attitude DBA 9055-7588 Qu�bec Inc.
NDC Product
Human Otc DrugAttitude - Lip Balm - Spf 15 - Coconut NDC 61649-985
- Generic Name
- Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Aurobindo Pharma Limited
NDC Product
Drug For Further Processing- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 59651-823
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 59651-824
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 59651-825
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 59651-826
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugClarithromycin NDC 65862-225
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClarithromycin NDC 65862-226
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 65862-402
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 65862-403
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 65862-959
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvPAK
NDC Product
Human Prescription DrugClarithromycin NDC 50268-178
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClarithromycin NDC 50268-179
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMesalamine NDC 50268-577
- Generic Name
- Mesalamine
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline NDC 50268-768
- Generic Name
- Sertraline
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline NDC 50268-769
- Generic Name
- Sertraline
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline NDC 50268-770
- Generic Name
- Sertraline
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 50268-823
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 50268-824
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 50268-825
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
BEL STAR S A
NDC Product
Human Otc DrugLbel Solutions Pro Hialuron Balm Balsamo Labial Hidratante 72h Fps 20 Hydrating Lip Balm 72h Spf 20 Berry Universel NDC 14141-350
- Generic Name
- Octinoxate, Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLbel Solutions Pro Hialuron Balm Balsamo Labial Hidratante 72h Fps 20 Hydrating Lip Balm 72h Spf 20 Coral Universel NDC 14141-351
- Generic Name
- Octinoxate, Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLbel Solutions Pro Hialuron Balm Balsamo Labial Hidratante 72h Fps 20 Hydrating Lip Balm 72h Spf 20 Nude Universel NDC 14141-352
- Generic Name
- Octinoxate, Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLbel Solutions Pro Hialuron Balm Balsamo Labial Hidratante 72h Fps 20 Hydrating Lip Balm 72h Spf 20 Rose Universel NDC 14141-353
- Generic Name
- Octinoxate, Zinc Oxide
- Dosage Form
- Stick
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
BEL STAR SA
NDC Product
Human Otc DrugCyzone Trax Desodorante Antitranspirante Roll On NDC 14141-458
- Generic Name
- Aluminum Sesquichlorohydrate
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCyzone Nitro Desodorante Antitranspirante Roll On NDC 14141-460
- Generic Name
- Aluminum Sesquichlorohydrate
- Dosage Form
- Emulsion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Bali Body Pty Ltd
NDC Product
Human Otc DrugBali Body Sheer Glow Sunscreen Spf 50 NDC 70630-0040
- Generic Name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Bentley Laboratories, LLC
NDC Product
Human Otc DrugCoola Refreshing Water Mist Spf 18 NDC 54111-148
- Generic Name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage Form
- Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Bionpharma Inc.
NDC Product
Human Prescription DrugCimetidine NDC 69452-323
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 69452-324
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 69452-325
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 69452-326
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
BluePoint Laboratories
NDC Product
Human Prescription DrugDivalproex Sodium NDC 68001-472
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 68001-473
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 68001-474
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Borden Company (Private) Limited
NDC Product
Human Otc DrugEagle Green Balm NDC 43405-100
- Generic Name
- Camphor Menthol
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Bryant Ranch Prepack
NDC Product
Human Prescription DrugDivalproex Sodium NDC 63629-4278
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 71335-0008
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClarithromycin NDC 71335-0017
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 71335-2124
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 71335-2158
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 71335-2862
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 71335-2885
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 71335-3110
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline NDC 71335-9714
- Generic Name
- Sertraline
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 72162-2460
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
C.B. Fleet Company, Inc.
NDC Product
Human Otc DrugFleet NDC 0132-0400
- Generic Name
- Mineral Oil
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Carma Laboratories, Inc.
NDC Product
Human Otc DrugCarmex Classic Lip Balm Medicated NDC 10210-0022
- Generic Name
- Camphor (synthetic), Petrolatum
- Dosage Form
- Salve
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarmex Classic Lip Balm Medicated Spf 15 NDC 10210-0023
- Generic Name
- Octinoxate, Oxybenzone, Petrolatum
- Dosage Form
- Salve
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarmex Classic Lip Balm Medicated NDC 10210-0038
- Generic Name
- Camphor (synthetic), White Petrolatum
- Dosage Form
- Salve
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarmex Classic Lip Balm Medicated NDC 10210-0039
- Generic Name
- Camphor (synthetic), White Petrolatum
- Dosage Form
- Salve
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarmex Classic Lip Balm Medicated Free Wintergreen Stick NDC 10210-0047
- Generic Name
- Octinoxate, Oxybenzone, Camphor (synthetic), White Petrolatu...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarmex Classic Lip Balm Medicated Triple Force Formula NDC 10210-0053
- Generic Name
- White Petrolatum
- Dosage Form
- Salve
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarmex Classic Lip Balm Medicated Triple Force Formula NDC 10210-0054
- Generic Name
- White Petrolatum
- Dosage Form
- Salve
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarmex Classic Lip Balm Medicated Lip Protectant NDC 10210-0055
- Generic Name
- White Petrolatum
- Dosage Form
- Salve
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarmex Weather Guard Moisturizing Lip Balm Spf 30 NDC 10210-0056
- Generic Name
- Avobenzone, Homosalate, Octisalate, Octocrylene, White Petro...
- Dosage Form
- Salve
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarmex 10 Count Variety Pack Spf 15 Sunscreen NDC 10210-0057
- Generic Name
- Octinoxate, Oxybenzone, Petrolatum
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Camphor (synthetic), Petrolatum
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Octinoxate, Oxybenzone, White Petrolatum
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Camphor (synthetic), White Petrolatum, Octinoxate, Oxybenzon...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Camphor (synthetic), White Petrolatum, Octinoxate, Oxybenzon...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarmex Classic Lip Balm Medicated Spf15 Triple Force Formula NDC 10210-0066
- Generic Name
- Octinoxate, Oxybenzone, White Petrolatum
- Dosage Form
- Salve
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Camphor (synthetic), White Petrolatum, Octinoxate, Oxybenzon...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Camphor (synthetic), White Petrolatum, Octinoxate, Oxybenzon...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Camphor (synthetic), White Petrolatum, Octinoxate, Oxybenzon...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Camphor (synthetic), White Petrolatum Octinoxate, Oxybenzone...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarmex Classic Lip Balm Medicated NDC 10210-0096
- Generic Name
- Camphor (synthetic), White Petrolatum
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Chartwell Governmental & Specialty RX, LLC.
NDC Product
Human Prescription DrugCarbamazepine NDC 68999-802
- Generic Name
- Carbamazepine
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarbamazepine NDC 68999-867
- Generic Name
- Carbamazepine
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Chartwell RX, LLC
NDC Product
Human Prescription DrugCarbamazepine NDC 62135-802
- Generic Name
- Carbamazepine
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Coupler LLC
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 67046-1665
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Dade Paper & Bag, LLC
NDC Product
Human Otc DrugVictoria Bay Anti-bacterial Hand NDC 71907-301
- Generic Name
- Pmcx
- Dosage Form
- Soap
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Devatis Inc.
NDC Product
Human Prescription DrugAmoxicillin And Clavulanate Potassium NDC 73043-008
- Generic Name
- Amoxicillin And Clavulanate Potassium
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
DirectRx
NDC Product
Human Prescription DrugDivalproex Sodium NDC 61919-249
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Direct_Rx
NDC Product
Human Prescription DrugAlprazolam Odt C-iv NDC 72189-637
- Generic Name
- Alprazolam Odt C-iv
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClarithromycin NDC 72189-639
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Dr.Reddy's Laboratories Limited
NDC Product
Human Prescription DrugDivalproex Sodium NDC 55111-529
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 55111-530
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 55111-531
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
EO Products, LLC
NDC Product
Human Otc DrugEveryone Hand Sanitizer Coconut Lemon NDC 54748-301
- Generic Name
- Alcohol
- Dosage Form
- Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEveryone Hand Sanitizer Coconut Lemon NDC 54748-601
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEveryone Hand Sanitizer Wipes Coconut Lemon NDC 54748-701
- Generic Name
- Ethyl Alcohol
- Dosage Form
- Cloth
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugEx-lax Regular Strength Chocolated Stimulant Laxative NDC 0067-8140
- Generic Name
- Sennosides
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Jack Black L.L.C.
NDC Product
Human Otc DrugJack Black NDC 66738-171
- Generic Name
- Avobenzone/homosalate/octisalate/petrolatum
- Dosage Form
- Ointment
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
June Jacobs Labs, LLC
NDC Product
Human Otc DrugLip Renewal Spf 50 NDC 65278-105
- Generic Name
- Avobenzone, Homosalate, Octinoxate, Octisalate
- Dosage Form
- Paste
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Lupin Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugWymzya Fe NDC 68180-873
- Generic Name
- Norethindrone And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugKaitlib Fe NDC 68180-903
- Generic Name
- Norethindrone And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
Major Pharmaceuticals
NDC Product
Human Prescription DrugClarithromycin NDC 0904-6872
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Medline Industries, LP
NDC Product
Human Otc DrugRemedy Nutrashield NDC 53329-157
- Generic Name
- Dimethicone
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRemedy Antifungal With Olivamine NDC 53329-162
- Generic Name
- Miconazole Nitrate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRemedy Calazime Skin Protectant NDC 53329-165
- Generic Name
- Calamine, Menthol, White Petrolatum, Zinc Oxide
- Dosage Form
- Paste
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Mission Pharmacal Company
NDC Product
Human Prescription DrugCitranatal Assure NDC 0178-0891
- Generic Name
- Ascorbic Acid, Calcium Citrate, Iron, Vitamin D, Dl- Alpha- ...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugCimetidine NDC 0378-0053
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 0378-0317
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 0378-0372
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 0378-0541
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPhenytoin NDC 59762-0531
- Generic Name
- Phenytoin
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 0615-8596
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 0615-8603
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 0615-8604
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Northwind Health Company, LLC
NDC Product
Human Prescription DrugDivalproex Sodium NDC 51655-365
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 51655-697
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NuCare Pharmaceuticals,Inc.
NDC Product
Human Prescription DrugSertraline NDC 68071-3534
- Generic Name
- Sertraline
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline NDC 68071-3626
- Generic Name
- Sertraline
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClarithromycin NDC 68071-5045
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
PD-Rx Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugClarithromycin NDC 43063-823
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 55289-581
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Par Health USA, LLC
NDC Product
Human Prescription DrugAlprazolam NDC 49884-110
- Generic Name
- Alprazolam
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlprazolam NDC 49884-111
- Generic Name
- Alprazolam
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlprazolam NDC 49884-213
- Generic Name
- Alprazolam
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlprazolam NDC 49884-214
- Generic Name
- Alprazolam
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugNurtec Odt NDC 72618-3000
- Generic Name
- Rimegepant Sulfate
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- NDA
Active Listing
Pollock Investments Inc
NDC Product
Human Otc DrugAnti-bacterial Hand NDC 71925-301
- Generic Name
- Pcmx
- Dosage Form
- Soap
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Preferred Pharmaceuticals Inc.
NDC Product
Human Prescription DrugClarithromycin NDC 68788-8480
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Proficient Rx LP
NDC Product
Human Prescription DrugClarithromycin NDC 63187-625
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 63187-742
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 63187-743
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
REMEDYREPACK INC.
NDC Product
Human Prescription DrugClarithromycin NDC 70518-0204
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 70518-2357
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 70518-2626
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 70518-3055
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 70518-3683
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 70518-4518
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 70518-4575
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 70518-4590
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSertraline Hydrochloride NDC 70518-4606
- Generic Name
- Sertraline Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
REVLON
NDC Product
Human Otc DrugEight Hour Skin Fragrance Free NDC 10967-673
- Generic Name
- Petrolatum
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rising Pharma Holdings, Inc.
NDC Product
Human Prescription DrugLansoprazole, Amoxicillin, Clarithromycin NDC 57237-001
- Generic Name
- Lansoprazole, Amoxicillin, Clarithromycin
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClarithromycin NDC 57237-044
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClarithromycin NDC 57237-045
- Generic Name
- Clarithromycin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 57237-047
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 57237-048
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 57237-106
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
ST. MARY'S MEDICAL PARK PHARMACY
NDC Product
Human Prescription DrugDivalproex Sodium NDC 60760-698
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
The Procter & Gamble Manufacturing Company
NDC Product
Human Otc Drug- Generic Name
- Colloidal Oatmeal
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Colloidal Oatmeal
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Tom's of Maine, Inc.
NDC Product
Human Otc Drug- Generic Name
- Sodium Monofluorophosphate
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Sodium Monofluorophosphate
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Trader Joe's Company
NDC Product
Human Otc DrugTrader Joes Shimmer Sunscreen Broad Spectrum Spf 30 NDC 71270-163
- Generic Name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage Form
- Oil
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Unichem Pharmaceuticals (USA), Inc.
NDC Product
Human Prescription DrugDivalproex Sodium NDC 29300-138
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 29300-139
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 29300-140
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Viatris Specialty LLC
NDC Product
Human Prescription DrugDilantin-125 NDC 58151-115
- Generic Name
- Phenytoin
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
