NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Mint Flavor NDC 17856-1362
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Sodium Carbonate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 45P3261C7T.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 497-19-8 and the RxNorm Concept ID (RxCUI) 36685. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
SODIUM CARBONATE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
45P3261C7T
The specific atomic composition represented as a molecular structure string.
InChIKey
CO3.2Na International Chemical Identifier digital signature for unique molecular identification.
SMILES String
CDBYLPFSWZWCQE-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
[O-]C([O-])=O.[Na+].[Na+]
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Sodium Carbonate. 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
SODIUM CARBONATE
OF
Common Names & Synonyms
ANHYDROUS SODIUM CARBONATE
CN
CARBONIC ACID SODIUM SALT (1:2)
CN
CARBONIC ACID, DISODIUM SALT
CN
DRIED SODIUM CARBONATE [JAN]
CN
NATRUM CARBONICUM
CN
NATRUM CARBONICUM [HPUS]
CN
SODA ASH
CN
SODA ASH [II]
CN
SODA-ASH
CN
SODIUM CARBONATE (ANHYDROUS)
CN
SODIUM CARBONATE [EP MONOGRAPH]
CN
SODIUM CARBONATE [FCC]
CN
SODIUM CARBONATE [HSDB]
CN
SODIUM CARBONATE [II]
CN
SODIUM CARBONATE [MART.]
CN
SODIUM CARBONATE [MI]
CN
SODIUM CARBONATE [ORANGE BOOK]
CN
SODIUM CARBONATE [VANDF]
CN
SODIUM CARBONATE [WHO-DD]
CN
SODIUM CARBONATE ANHYDROUS
CN
SODIUM CARBONATE ANHYDROUS [MART.]
CN
SODIUM CARBONATE ANHYDROUS [USP-RS]
CN
SODIUM CARBONATE, ANHYDROUS
CN
SODIUM CARBONATE, ANHYDROUS [EP IMPURITY]
CN
SODIUM SALT OF CARBONIC ACID
CN
SOLVAY SODA
CN
Systematic Nomenclature
DISODIUM CARBONATE
SYS
Technical Codes
E-500(I)
CD
INS NO.500(I)
CD
INS-500(I)
CD
NSC-156204
CD
NDC Products Containing SODIUM CARBONATE
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
ATLANTIC BIOLOGICALS CORP.
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Original Flavor NDC 17856-3030
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
AbbVie Inc.
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
Ajanta Pharma USA Inc.
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 27241-256
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
Alcon Laboratories, Inc.
NDC Product
Human Prescription DrugCyclomydril NDC 0065-0359
- Generic Name
- Cyclopentolate Hydrochloride And Phenylephrine Hydrochloride
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclogyl NDC 0065-0395
- Generic Name
- Cyclopentolate Hydrochloride
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclogyl NDC 0065-0396
- Generic Name
- Cyclopentolate Hydrochloride
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclogyl NDC 0065-0397
- Generic Name
- Cyclopentolate Hydrochloride
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- ANDA
Active Listing
Allergan, Inc.
NDC Product
Human Prescription DrugAvycaz NDC 0456-2700
- Generic Name
- Ceftazidime, Avibactam
- Dosage Form
- Powder, For Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
Amerisource Bergen
NDC Product
Human Otc DrugGood Neighbor Pharmacy Nicotine NDC 24385-598
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bausch & Lomb Incorporated
NDC Product
Human Prescription DrugCyclopentolate Hydrochloride NDC 24208-735
- Generic Name
- Cyclopentolate Hydrochloride
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- ANDA
Active Listing
Boiron
NDC Product
Human Otc DrugNatrum Carbonicum NDC 0220-3531
- Generic Name
- Sodium Carbonate
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugNatrum Carbonicum NDC 0220-3532
- Generic Name
- Sodium Carbonate
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugNatrum Carbonicum NDC 0220-3533
- Generic Name
- Sodium Carbonate
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugNatrum Carbonicum NDC 0220-3534
- Generic Name
- Sodium Carbonate
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugNatrum Carbonicum NDC 0220-3535
- Generic Name
- Sodium Carbonate
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugNatrum Carbonicum NDC 0220-3536
- Generic Name
- Sodium Carbonate
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugNatrum Carbonicum NDC 0220-3537
- Generic Name
- Sodium Carbonate
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugNatrum Carbonicum NDC 0220-3538
- Generic Name
- Sodium Carbonate
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugNatrum Carbonicum NDC 0220-3577
- Generic Name
- Sodium Carbonate
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Church & Dwight Co., Inc.
NDC Product
Human Otc DrugPeroxicare NDC 10237-655
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEnamel Defense NDC 10237-666
- Generic Name
- Sodium Fluoride
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEssentials Healthy Teeth And Gums NDC 10237-670
- Generic Name
- Sodium Fluoride 0.24%
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEssentials Whiten And Strengthen NDC 10237-672
- Generic Name
- Sodium Fluoride 0.24%
- Dosage Form
- Paste, Dentifrice
- Route
- Dental
- Marketing
- OTC MONOGRAPH DRUG
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
Guna spa
NDC Product
Human Otc DrugGuna-bowel NDC 17089-293
- Generic Name
- Aloe - Aluminum Oxide - Bryonia Alba Root - Chelidonium Maju...
- Dosage Form
- Solution/ Drops
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc DrugGuna Bowel Plus NDC 17089-470
- Generic Name
- Activated Charcoal - Aloe - Aluminum Oxide - Bryonia Alba Ro...
- Dosage Form
- Solution/ Drops
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugNicorette Original NDC 0135-0157
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Original NDC 0135-0158
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Mint NDC 0135-0229
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Mint NDC 0135-0230
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Fruit Chill NDC 0135-0241
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Fruit Chill NDC 0135-0242
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Spearmint Burst NDC 0135-0355
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Cinnamon Surge NDC 0135-0466
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Cinnamon Surge NDC 0135-0467
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette White Ice Mint NDC 0135-0474
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette White Ice Mint NDC 0135-0475
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-0508
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-0510
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-0511
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Spearmint Burst NDC 0135-0532
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Spearmint Burst NDC 0135-0533
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-0625
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-0626
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-0635
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-0636
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-1500
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette NDC 0135-2800
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Peppermint NDC 0135-8050
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Peppermint NDC 0135-8060
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Cherry Peppermint NDC 0135-8070
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugNicorette Cherry Peppermint NDC 0135-8071
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- NDA
Active Listing
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
NDC Product
Human Prescription DrugMethohexital Sodium NDC 23155-893
- Generic Name
- Methohexital Sodium
- Dosage Form
- Injection
- Route
- Intramuscular; Intravenous; Rectal
- Marketing
- ANDA
Active Listing
Hospira, Inc.
NDC Product
Human Prescription DrugTazicef NDC 0409-5082
- Generic Name
- Ceftazidime
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intramuscular; Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTazicef NDC 0409-5084
- Generic Name
- Ceftazidime
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTazicef NDC 0409-5086
- Generic Name
- Ceftazidime
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTazicef NDC 0409-5092
- Generic Name
- Ceftazidime
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTazicef NDC 0409-5093
- Generic Name
- Ceftazidime
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0029
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0053
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0170
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine Mint NDC 0113-0206
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0344
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0422
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0456
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0532
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0734
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0854
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0873
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-0957
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-1125
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-1190
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-1352
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-2502
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-4111
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-5023
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-6020
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-7020
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-7031
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-7999
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-8100
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Nicotine NDC 0113-8600
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
Major Pharmaceuticals
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0904-6290
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0904-6291
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0904-6292
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0904-6293
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 0904-6870
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Medicure International Inc
NDC Product
Human Prescription DrugZypitamag NDC 25208-201
- Generic Name
- Pitavastatin Magnesium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZypitamag NDC 25208-202
- Generic Name
- Pitavastatin Magnesium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0378-3950
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0378-3951
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0378-3952
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0378-3953
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4513
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4514
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4515
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4516
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4517
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4518
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4519
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmlodipine And Atorvastatin NDC 0378-4520
- Generic Name
- Amlodipine And Atorvastatin
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 0378-6688
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 0378-6689
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 0615-7629
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0615-8006
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0615-8007
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0615-8008
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 0615-8009
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 0615-8113
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NORTHSTAR RX LLC
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 16714-173
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 16714-174
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 16714-175
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtorvastatin Calcium NDC 16714-176
- Generic Name
- Atorvastatin Calcium
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rite Aid Corporation
NDC Product
Human Otc DrugNicotine NDC 11822-0009
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 11822-0124
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 11822-0201
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 11822-0344
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 11822-0424
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 11822-0873
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMini Nicotine NDC 11822-0957
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 11822-1649
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 11822-1720
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rugby Laboratories
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Mint Flavor NDC 0536-1362
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Mint Flavor NDC 0536-1372
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Original Flavor NDC 0536-3029
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Original Flavor NDC 0536-3030
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Coated Mint Flavor NDC 0536-3112
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Coated Mint Flavor NDC 0536-3113
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Coated Fruit Flavor NDC 0536-3386
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRugby Nicotine Polacrilex Gum, Coated Fruit Flavor NDC 0536-3387
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Polacrilex NDC 0536-3404
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Polacrilex NDC 0536-3405
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
Rugby Laboratories, Inc.
NDC Product
Human Otc DrugNicotine NDC 0536-1337
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugMaxi Nicotine NDC 0536-1338
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
Safeway
NDC Product
Human Otc DrugSignature Care Nicotine NDC 21130-172
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSignature Care Nicotine NDC 21130-173
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSignature Care Nicotine NDC 21130-185
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSignature Care Nicotine NDC 21130-186
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSignature Care Nicotine NDC 21130-211
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSignature Care Nicotine NDC 21130-269
- Generic Name
- Nicotine
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 21130-389
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSignature Care Nicotine NDC 21130-522
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 21130-636
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSignature Care Nicotine NDC 21130-700
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSignature Care Nicotine NDC 21130-820
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sagent Pharmaceuticals
NDC Product
Human Prescription DrugCeftazidime NDC 25021-127
- Generic Name
- Ceftazidime
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intramuscular; Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCeftazidime NDC 25021-128
- Generic Name
- Ceftazidime
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCeftazidime NDC 25021-129
- Generic Name
- Ceftazidime
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeropenem NDC 25021-160
- Generic Name
- Meropenem
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeropenem NDC 25021-161
- Generic Name
- Meropenem
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
TRP Company
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
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugSprintec NDC 0555-9016
- Generic Name
- Norgestimate And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTri-sprintec NDC 0555-9018
- Generic Name
- Norgestimate And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- ANDA
Active Listing
Torrent Pharmaceuticals Limited
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 13668-096
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 13668-429
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREENS CO.
NDC Product
Human Otc DrugWalgreen Liquid Antacid NDC 0363-6701
- Generic Name
- Calcium Carbonate, Magnesium Hydroxide And Simethicone
- Dosage Form
- Suspension
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Walgreen Company
NDC Product
Human Otc DrugNicotine NDC 0363-0124
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-0201
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-0411
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-0424
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-0456
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Mini NDC 0363-0734
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-0873
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-0919
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-1012
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Mini NDC 0363-1130
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-1825
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-2309
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-4049
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-4190
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Mini NDC 0363-6011
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-7044
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-7050
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Mini NDC 0363-7051
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-7103
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-7269
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-7971
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreens
NDC Product
Human Otc DrugNicotine Polacrilex Mint NDC 0363-1420
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Polacrilex Mint NDC 0363-1421
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Polacrilex Original NDC 0363-1608
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine Polacrilex Original NDC 0363-1609
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Buccal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-3911
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-5760
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-9290
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-9350
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Gum, Chewing
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-9620
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugNicotine NDC 0363-9780
- Generic Name
- Nicotine Polacrilex
- Dosage Form
- Lozenge
- Route
- Oral
- Marketing
- ANDA
Active Listing
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
NDC Product
Human Prescription DrugProtonix Delayed-release NDC 0008-0841
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugProtonix Delayed-release NDC 0008-0843
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugProtonix Delayed-release NDC 0008-0844
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
