NDC Product
Human Prescription DrugSynthroid NDC 0074-3727
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Fd&c Blue No. 1, uniquely identified by the FDA Unique Ingredient Identifier (UNII) H3R47K3TBD.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 3844-45-9 and the RxNorm Concept ID (RxCUI) 1310605. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
FD&C BLUE NO. 1
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
H3R47K3TBD
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
Substance Type
mixture
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Fd&c Blue No. 1. 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
ACID BLUE 9
OF
AO1
OF
AO205
OF
BLUE 1
OF
CI 42090
OF
Common Names & Synonyms
BENZENEMETHANAMINIUM, N-ETHYL-N-(4-((4-(ETHYL((3-SULFOPHENYL)METHYL)AMINO)PHENYL)(2-SULFOPHENYL)METHYLENE)-2,5-CYCLOHEXADIEN-1-YLIDENE)-3-SULFO-, INNER SALT, SODIUM SALT
CN
BLUE NO. 1
CN
BRILLIANT BLUE
CN
BRILLIANT BLUE [FCC]
CN
BRILLIANT BLUE FCF
CN
BRILLIANT BLUE FCF [MART.]
CN
BRILLIANT BLUE FCF [MI]
CN
BRILLIANT BLUE FCF [WHO-DD]
CN
CI-FOOD BLUE 2
CN
D&C BLUE NO. 1
CN
D&C BLUE NO. 1 [II]
CN
DYE BRILLIANT BLUE
CN
DYE FDC BLUE #1 [VANDF]
CN
E133
CN
F D & C BLUE #1 [VANDF]
CN
F D & C BLUE #1 ALUMINUM LAKE [VANDF]
CN
F D & C BLUE #1 LAKE [VANDF]
CN
F D & C BLUE NO. 1
CN
F D & C YELLOW BLUE #1 [VANDF]
CN
FD&C BLUE NO. 1
CN
FD&C BLUE NO. 1 [FCC]
CN
FD&C BLUE NO. 1 [II]
CN
FDC BLUE NO. 1
CN
N-ETHYL-N-(4-((4-(ETHYL((3-SULFOPHENYL)METHYL)AMINO)PHENYL)(2-SULFOPHENYL)METHYLENE)-2,5-CYCLOHEXADIEN-1-YLIDENE)-3-SULFOBENZENEMETHANAMINIUM HYDROXIDE, INNER SALT, DISODIUM SALT
CN
Brand / Trade Names
COVACAP BLEU W 6102
BN
VIBRACOLOR BLUE ABL9
BN
Technical Codes
CI-(1975)NO.42900
CD
E-133
CD
FOOD BLUE 2
CD
INS NO.133
CD
INS-133
CD
JAPAN BLUE 1
CD
NDC Products Containing FD&C BLUE NO. 1
This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory:
Manufacturer Quick Index
Note: Due to the high number of listings (500), only Active Listings are currently displayed. Display is limited to the first 200 products.
Showing 200 active products
AbbVie Inc.
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-4341
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-4552
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-5182
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugDepakote Sprinkles NDC 0074-6114
- Generic Name
- Divalproex Sodium
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-6594
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-6624
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-7068
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-7069
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-7070
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-7148
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-7149
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSynthroid NDC 0074-9296
- Generic Name
- Levothyroxine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA
Active Listing
Allergan, Inc.
NDC Product
Human Prescription DrugTaytulla NDC 0023-5862
- Generic Name
- Norethindrone Acetate And Ethinyl Estradiol, And Ferrous Fum...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
Eli Lilly and Company
NDC Product
Human Prescription DrugRetevmo NDC 0002-2980
- Generic Name
- Selpercatinib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc DrugRobitussin Day And Night Cough Relief Value Pack NDC 0031-2099
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, Chlorpheniramine...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Day And Night Maximum Strength Cough Dm NDC 0031-2103
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, Doxylamine Succi...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Day And Night Cough Relief Dm Max NDC 0031-2834
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin, Doxylamine Succi...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin Cough And Chest Congestion Dm NDC 0031-8702
- Generic Name
- Dextromethorphan Hydrobromide And Guaifenesin
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin Cough And Chest Congestion Dm NDC 0031-8715
- Generic Name
- Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Maximum Strength Nighttime Cough Dm NDC 0031-8718
- Generic Name
- Dextromethorphan Hydrobromide, Doxylamine Succinate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugChildrens Robitussin 12 Hour Cough Relief NDC 0031-8726
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Long-acting Coughgels NDC 0031-8743
- Generic Name
- Dextromethorphan Hydrobromide
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, And Doxylamine...
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin 12 Hour Cough Relief NDC 0031-8753
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRobitussin 12 Hour Cough Relief NDC 0031-8755
- Generic Name
- Dextromethorphan Polistirex
- Dosage Form
- Suspension, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRobitussin Cough Plus Chest Congestion Dm NDC 0031-8757
- Generic Name
- Dextromethorphan Hydrobromide And Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Direct Cough NDC 0031-9302
- Generic Name
- Dextromethorphan Hydrobromide
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime NDC 0067-0100
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime Honey Ginger NDC 0067-0103
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Chest Congestion Daytime NDC 0067-0104
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Nighttime NDC 0067-0105
- Generic Name
- Acetaminophen, Diphenhydramine Hcl
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime Berry Burst NDC 0067-0106
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief NDC 0067-0107
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Diphenphydramine Hcl, G...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Combo Pack NDC 0067-0122
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Diphenhydramine Hcl
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Combo Pack NDC 0067-0123
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Diphenhydramine Hcl
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Extra Strength Pain Reliever NDC 0067-2001
- Generic Name
- Acetaminophen, Aspirin (nsaid), And Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Extra Strength Headache NDC 0067-2002
- Generic Name
- Acetaminophen, Aspirin (nsaid), Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Extra Strength Headache NDC 0067-2003
- Generic Name
- Acetaminophen, Aspirin (nsaid), Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Extra Strength Geltabs NDC 0067-2021
- Generic Name
- Acetaminophen, Asprin, Caffeine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Migraine Geltabs NDC 0067-2035
- Generic Name
- Acetaminophen, Asprin, Caffeine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugExcedrin Migraine NDC 0067-2039
- Generic Name
- Acetaminophen, Aspirin (nsaid) And Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugExcedrin Migraine NDC 0067-2040
- Generic Name
- Acetaminophen, Aspirin, And Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugExcedrin Migraine Relief NDC 0067-2042
- Generic Name
- Acetaminophen, Aspirin (nsaid), Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugExcedrin Pm Triple Action Caplets NDC 0067-2056
- Generic Name
- Acetaminophen, Aspirin (nsaid) And Diphenhydramine Citrate
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Powerpods Daytime Severe Cold NDC 0067-6094
- Generic Name
- Acetaminophen, Dextromethorphan, Phenylephrine
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Powerpods Nighttime Severe Cold NDC 0067-6095
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGas-x Extra Strength Softgels NDC 0067-6275
- Generic Name
- Simethicone
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGas-x Maximum Strength Softgels NDC 0067-6283
- Generic Name
- Simethicone
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Multi-symptom Severe Cold NDC 0067-6426
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime Berry Burst NDC 0067-6800
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hydrochlo...
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Daytime NDC 0067-6802
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Nighttime NDC 0067-6803
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl, Diph...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Daytime Severe Cold And Cough NDC 0067-7917
- Generic Name
- Acetaminophen, Dextromethorphan, Phenylephrine
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Nighttime Severe Cold And Cough NDC 0067-7918
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl, Diph...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Flu Relief Max Strength Daytime NDC 0067-7921
- Generic Name
- Acetaminophen, Dextromethorphan Hbr
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Flu Relief Max Strength Nighttime NDC 0067-7922
- Generic Name
- Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hb...
- Dosage Form
- Powder
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, And Acetaminophen, Chlo...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Daytime Nighttime Value Pack NDC 0067-8125
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl And A...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Daytime Severe Cold And Cough NDC 0067-8127
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Nighttime Severe Cold And Cough NDC 0067-8129
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Severe Cold And Flu Syrup NDC 0067-8132
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephr...
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Tension Headache NDC 0067-8139
- Generic Name
- Acetaminophen, Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEx-lax Maximum Strength Stimulant Laxative NDC 0067-8142
- Generic Name
- Sennosides
- Dosage Form
- Pill
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Aspirin (nsaid), Caffeine, And Diphenhydramin...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Aspirin (nsaid), Caffeine, And Diphenhydramin...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Extra Strength And Excedrin Tension Headache NDC 0067-8151
- Generic Name
- Acetaminophen, Aspirin (nsaid), And Caffeine
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Migraine NDC 0067-8201
- Generic Name
- Acetaminophen, Aspirin (nsaid) And Caffeine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Powder, For Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Hikma Pharmaceuticals USA Inc
NDC Product
Human Prescription DrugImipramine Pamoate NDC 0054-0273
- Generic Name
- Imipramine Pamoate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImipramine Pamoate NDC 0054-0274
- Generic Name
- Imipramine Pamoate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImipramine Pamoate NDC 0054-0275
- Generic Name
- Imipramine Pamoate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugImipramine Pamoate NDC 0054-0276
- Generic Name
- Imipramine Pamoate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugBalsalazide Disodium NDC 0054-0079
- Generic Name
- Balsalazide Disodium
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZaleplon NDC 0054-0084
- Generic Name
- Zaleplon
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZaleplon NDC 0054-0085
- Generic Name
- Zaleplon
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCalcium Acetate NDC 0054-0088
- Generic Name
- Calcium Acetate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRamipril NDC 0054-0108
- Generic Name
- Ramipril
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRamipril NDC 0054-0109
- Generic Name
- Ramipril
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGalantamine Hydrobromide NDC 0054-0137
- Generic Name
- Galantamine Hydrobromide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMycophenolate Mofetil NDC 0054-0163
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMycophenolate Mofetil NDC 0054-0166
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0372
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0373
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0374
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLisdexamfetamine Dimesylate NDC 0054-0375
- Generic Name
- Lisdexamfetamine Dimesylate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclophosphamide NDC 0054-0382
- Generic Name
- Cyclophosphamide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCyclophosphamide NDC 0054-0383
- Generic Name
- Cyclophosphamide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugDesvenlafaxine NDC 0054-0400
- Generic Name
- Desvenlafaxine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDesvenlafaxine NDC 0054-0401
- Generic Name
- Desvenlafaxine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDesvenlafaxine NDC 0054-0603
- Generic Name
- Desvenlafaxine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Butalbital, Acetaminophen, Caffeine And Codeine Phosphate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlvimopan NDC 0054-0668
- Generic Name
- Alvimopan
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDicyclomine Hydrochloride NDC 0054-0748
- Generic Name
- Dicyclomine Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Butalbital, Acetaminophen, Caffeine And Codeine Phosphate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugDexamethasone Intensol NDC 0054-3176
- Generic Name
- Dexamethasone Intensol
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-3177
- Generic Name
- Dexamethasone
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4180
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4181
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4182
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4183
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4184
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-4186
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8174
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8175
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8176
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8179
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8180
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8181
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8183
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugBelsomra NDC 0006-0033
- Generic Name
- Suvorexant
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBelsomra NDC 0006-0325
- Generic Name
- Suvorexant
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugBelsomra NDC 0006-0335
- Generic Name
- Suvorexant
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugNorpace Cr NDC 0025-2732
- Generic Name
- Disopyramide Phosphate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNorpace Cr NDC 0025-2742
- Generic Name
- Disopyramide Phosphate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNorpace NDC 0025-2762
- Generic Name
- Disopyramide Phosphate
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLitfulo NDC 0069-0334
- Generic Name
- Ritlecitinib
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugXeljanz Xr NDC 0069-0502
- Generic Name
- Tofacitinib
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugXeljanz NDC 0069-1002
- Generic Name
- Tofacitinib
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugXeljanz NDC 0069-1029
- Generic Name
- Tofacitinib
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugVyndamax NDC 0069-8730
- Generic Name
- Tafamidis
- Dosage Form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing
- NDA
Active Listing
Pharmacia & Upjohn Company LLC
NDC Product
Human Prescription DrugCleocin Hydrochloride NDC 0009-0225
- Generic Name
- Clindamycin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCleocin Hydrochloride NDC 0009-0331
- Generic Name
- Clindamycin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugCleocin Hydrochloride NDC 0009-0395
- Generic Name
- Clindamycin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugLovastatin NDC 0093-0576
- Generic Name
- Lovastatin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPiroxicam NDC 0093-0756
- Generic Name
- Piroxicam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPiroxicam NDC 0093-0757
- Generic Name
- Piroxicam
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNortriptyline Hydrochloride NDC 0093-0810
- Generic Name
- Nortriptyline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNortriptyline Hydrochloride NDC 0093-0811
- Generic Name
- Nortriptyline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNortriptyline Hydrochloride NDC 0093-0812
- Generic Name
- Nortriptyline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNortriptyline Hydrochloride NDC 0093-0813
- Generic Name
- Nortriptyline Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLovastatin NDC 0093-0928
- Generic Name
- Lovastatin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcitretin NDC 0093-1135
- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugAcitretin NDC 0093-1136
- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcitretin NDC 0093-1138
- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Acitretin
- Dosage Form
- Capsule
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1714
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1715
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1716
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1718
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1720
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugWarfarin Sodium NDC 0093-1721
- Generic Name
- Warfarin Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclobenzaprine Hydrochloride NDC 0093-1921
- Generic Name
- Cyclobenzaprine Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-2267
- Generic Name
- Amoxicillin
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-2268
- Generic Name
- Amoxicillin
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-3107
- Generic Name
- Amoxicillin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-3109
- Generic Name
- Amoxicillin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDicloxacillin Sodium NDC 0093-3123
- Generic Name
- Dicloxacillin Sodium
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDicloxacillin Sodium NDC 0093-3125
- Generic Name
- Dicloxacillin Sodium
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDisopyramide Phosphate NDC 0093-3127
- Generic Name
- Disopyramide Phosphate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDisopyramide Phosphate NDC 0093-3129
- Generic Name
- Disopyramide Phosphate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCamrese NDC 0093-3134
- Generic Name
- Levonorgestrel / Ethinyl Estradiol And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugCephalexin NDC 0093-3145
- Generic Name
- Cephalexin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCephalexin NDC 0093-3147
- Generic Name
- Cephalexin
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefdinir NDC 0093-3160
- Generic Name
- Cefdinir
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCefadroxil NDC 0093-3196
- Generic Name
- Cefadroxil
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClonazepam NDC 0093-3212
- Generic Name
- Clonazepam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClonazepam NDC 0093-3213
- Generic Name
- Clonazepam
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 0093-3544
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 0093-3545
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 0093-3546
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 0093-3547
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtomoxetine NDC 0093-3548
- Generic Name
- Atomoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrazosin Hydrochloride NDC 0093-4068
- Generic Name
- Prazosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrazosin Hydrochloride NDC 0093-4069
- Generic Name
- Prazosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAmoxicillin NDC 0093-4155
- Generic Name
- Amoxicillin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCephalexin NDC 0093-4175
- Generic Name
- Cephalexin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCephalexin NDC 0093-4177
- Generic Name
- Cephalexin
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5045
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5046
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 0093-5346
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 0093-5347
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 0093-5348
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine And Fluoxetine NDC 0093-5503
- Generic Name
- Olanzapine And Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine And Fluoxetine NDC 0093-5504
- Generic Name
- Olanzapine And Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine And Fluoxetine NDC 0093-5505
- Generic Name
- Olanzapine And Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine And Fluoxetine NDC 0093-5506
- Generic Name
- Olanzapine And Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOlanzapine And Fluoxetine NDC 0093-5507
- Generic Name
- Olanzapine And Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtazanavir Sulfate NDC 0093-5526
- Generic Name
- Atazanavir Sulfate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtazanavir Sulfate NDC 0093-5527
- Generic Name
- Atazanavir Sulfate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAtazanavir Sulfate NDC 0093-5528
- Generic Name
- Atazanavir Sulfate
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5550
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5551
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5552
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5553
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5554
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5562
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRivelsa NDC 0093-6031
- Generic Name
- Levonorgestrel/ethinyl Estradiol And Ethinyl Estradiol
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 0093-7164
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugFluoxetine NDC 0093-7198
- Generic Name
- Fluoxetine
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMycophenolate Mofetil NDC 0093-7334
- Generic Name
- Mycophenolate Mofetil
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLansoprazole NDC 0093-7350
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLansoprazole NDC 0093-7351
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
