NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 50090-5246
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Hypromellose 2208 (100000 Mpa.s), uniquely identified by the FDA Unique Ingredient Identifier (UNII) VM7F0B23ZI.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9004-65-3 and the RxNorm Concept ID (RxCUI) 1300448. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
HYPROMELLOSE 2208 (100000 MPA.S)
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
VM7F0B23ZI
The specific atomic composition represented as a molecular structure string.
Substance Type
polymer
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Hypromellose 2208 (100000 Mpa.s). 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.
Common Names & Synonyms
HPMC 2208 (100000 CPS)
CN
HYDROXYPROPYL METHYLCELLULOSE 2208 (100000 CPS)
CN
HYDROXYPROPYL METHYLCELLULOSE 2208 (80000-120000 CPS)
CN
HYDROXYPROPYL METHYLCELLULOSE K100M
CN
HYPROMELLOSE 2208 (100000 CPS)
CN
HYPROMELLOSE 2208 (100000 MPA.S)
CN
HYPROMELLOSE 2208 (80000-120000 CPS)
CN
HYPROMELLOSE 2208 (80000-120000 CPS) [II]
CN
HYPROMELLOSE K100M
CN
Brand / Trade Names
BENECEL HPMC K100M
BN
METHOCEL K100M
BN
METHOCEL K100M PREMIUM
BN
METOLOSE 90SH 100000
BN
METOLOSE 90SH 100000SR
BN
NDC Products Containing HYPROMELLOSE 2208 (100000 MPA.S)
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 (214), only Active Listings are currently displayed.
Showing 169 active products
A-S Medication Solutions
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 50090-5396
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 50090-5397
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugJanumet Xr NDC 50090-5504
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 50090-5686
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 50090-5822
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 50090-6661
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 50090-6798
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 50090-6839
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 50090-7038
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 50090-7496
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 50090-7534
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 50090-7535
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 50090-7576
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 50090-7577
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 50090-7918
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aphena Pharma Solutions - Tennessee, LLC
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 71610-578
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 71610-772
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 71610-788
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 71610-825
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
AstraZeneca Pharmaceuticals LP
NDC Product
Human Prescription DrugXigduo Xr NDC 0310-6225
- Generic Name
- Dapagliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugXigduo Xr NDC 0310-6250
- Generic Name
- Dapagliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugXigduo Xr NDC 0310-6260
- Generic Name
- Dapagliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugXigduo Xr NDC 0310-6270
- Generic Name
- Dapagliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugXigduo Xr NDC 0310-6280
- Generic Name
- Dapagliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Aurobindo Pharma Limited
NDC Product
Human Prescription DrugNiacin NDC 59651-018
- Generic Name
- Niacin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNiacin NDC 59651-019
- Generic Name
- Niacin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugNiacin NDC 59651-020
- Generic Name
- Niacin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 59651-042
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 59651-043
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDapagliflozin And Metformin Hydrochloride NDC 59651-154
- Generic Name
- Dapagliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDapagliflozin And Metformin Hydrochloride NDC 59651-155
- Generic Name
- Dapagliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDapagliflozin And Metformin Hydrochloride NDC 59651-156
- Generic Name
- Dapagliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDapagliflozin And Metformin Hydrochloride NDC 59651-157
- Generic Name
- Dapagliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibric Acid NDC 59651-216
- Generic Name
- Fenofibric Acid
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFenofibric Acid NDC 59651-217
- Generic Name
- Fenofibric Acid
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 59651-539
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 59651-540
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 59651-541
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 59651-548
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 59651-549
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFesoterodine Fumarate NDC 65862-766
- Generic Name
- Fesoterodine Fumarate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFesoterodine Fumarate NDC 65862-767
- Generic Name
- Fesoterodine Fumarate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aurohealth LLC
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugPseudoephedrine Hydrochloride NDC 58602-884
- Generic Name
- Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bryant Ranch Prepack
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 63629-9147
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlfuzosin Hydrochloride NDC 63629-9155
- Generic Name
- Alfuzosin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 63629-9689
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 71335-1883
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 71335-2192
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 71335-2194
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 71335-2568
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 71335-9683
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 72162-1293
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
CVS Health Corp
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
CVS Pharmacy, Inc.
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugFesoterodine Fumarate NDC 31722-033
- Generic Name
- Fesoterodine Fumarate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFesoterodine Fumarate NDC 31722-034
- Generic Name
- Fesoterodine Fumarate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZileuton NDC 31722-044
- Generic Name
- Zileuton
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cardinal Health
NDC Product
Human Otc DrugFexofenadine Hydrochloride And Pseudoephedrine Hydrochloride NDC 70000-0677
- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cosco International, Inc.
NDC Product
Human Otc DrugCarpe Antiperspirant Underarm Fragrance Free NDC 52261-4713
- Generic Name
- Aluminum Sesquichlorohydrate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarpe Antiperspirant Underarm Vanilla Scent NDC 52261-4716
- Generic Name
- Aluminum Sesquichlorohydrate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarpe Antiperspirant Underarm Sandalwood Scent NDC 52261-4717
- Generic Name
- Aluminum Sesquichlorohydrate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarpe Antiperspirant Underarm Cucumber Splash Scent NDC 52261-4718
- Generic Name
- Aluminum Sesquichlorohydrate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarpe Antiperspirant Underarm Fresh Powder Scent NDC 52261-4719
- Generic Name
- Aluminum Sesquichlorohydrate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarpe Antiperspirant Underarm Rose Water Scent NDC 52261-4720
- Generic Name
- Aluminum Sesquichlorohydrate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarpe Antiperspirant Underarm NDC 52261-4721
- Generic Name
- Aluminum Sesquichlorohydrate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarpe Antiperspirant Underarm Mountain Breeze Scent NDC 52261-4722
- Generic Name
- Aluminum Sesquichlorohydrate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarpe Antiperspirant Underarm Warm Vanilla Scent NDC 52261-4726
- Generic Name
- Aluminum Sesquichlorohydrate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarpe Antiperspirant Underarm Lavender Citrus Scent NDC 52261-4727
- Generic Name
- Aluminum Sesquichlorohydrate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarpe Antiperspirant Underarm Coconut Vanilla Scent NDC 52261-4732
- Generic Name
- Aluminum Sesquichlorohydrate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarpe Antiperspirant Underarm Bergamot And Oud Scent NDC 52261-4733
- Generic Name
- Aluminum Sesquichlorohydrate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarpe Antiperspirant Underarm Clean Sport Scent NDC 52261-4734
- Generic Name
- Aluminum Sesquichlorohydrate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugCarpe Antiperspirant Underarm Cucumber Spa Scent NDC 52261-4735
- Generic Name
- Aluminum Sesquichlorohydrate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Coupler LLC
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 67046-1446
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 67046-1556
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
DIRECT RX
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 72189-132
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Direct_Rx
NDC Product
Human Prescription DrugDivalproex Sodium Er NDC 72189-459
- Generic Name
- Divalproex Sodium Er
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Dr.Reddys Laboratories Inc
NDC Product
Human Prescription DrugSaxagliptin And Metformin Hydrochloride NDC 43598-618
- Generic Name
- Saxagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSaxagliptin And Metformin Hydrochloride NDC 43598-619
- Generic Name
- Saxagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSaxagliptin And Metformin Hydrochloride NDC 43598-620
- Generic Name
- Saxagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Epic Pharma, LLC
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 42806-632
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 42806-633
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
GLENMARK PHARMACEUTICALS INC., USA
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 68462-520
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 68462-521
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Golden State Medical Supply, Inc.
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 51407-059
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 51407-208
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 51407-209
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 51407-210
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Guardian Drug Company
NDC Product
Human Otc DrugGuaifenesin Extended-release 600 Mg NDC 53041-233
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGuaifenesin Extended-release 1200 Mg NDC 53041-234
- Generic Name
- Guaifenesin
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Ingenus Pharmaceuticals, LLC
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 50742-175
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 50742-176
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 50742-177
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
KROGER COMPANY
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Kroger Company
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Laurus Labs Limited
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 42385-977
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 42385-978
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lupin Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugDivalproex Sodium NDC 68180-260
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 68180-261
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugJanumet Xr NDC 0006-0078
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugJanumet Xr NDC 0006-0080
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugJanumet Xr NDC 0006-0081
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Micro Labs Limited
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 42571-333
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 42571-334
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugDivalproex Sodium NDC 0615-8376
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 0615-8377
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NorthStar RxLLC
NDC Product
Human Prescription DrugZileuton NDC 72603-246
- Generic Name
- Zileuton
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFesoterodine Fumarate NDC 72603-413
- Generic Name
- Fesoterodine Fumarate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFesoterodine Fumarate NDC 72603-414
- Generic Name
- Fesoterodine Fumarate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Northwind Health Company, LLC
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 51655-077
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 51655-853
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugIsosorbide Mononitrate NDC 51655-922
- Generic Name
- Isosorbide Mononitrate
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlfuzosin Hydrochloride NDC 51655-967
- Generic Name
- Alfuzosin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Omnivium Pharmaceuticals LLC
NDC Product
Human Prescription DrugLevetiracetam Extended-release NDC 81665-100
- Generic Name
- Levetiracetam
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
PD-Rx Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 72789-049
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 72789-286
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 72789-472
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Prasco Laboratories
NDC Product
Human Prescription DrugDapagliflozin And Metformin Hydrochloride NDC 66993-361
- Generic Name
- Dapagliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugDapagliflozin And Metformin Hydrochloride NDC 66993-362
- Generic Name
- Dapagliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Preferred Pharmaceuticals Inc.
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 68788-8866
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Preferred Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugDivalproex Sodium NDC 68788-8358
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Proficient Rx LP
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 71205-667
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 71205-686
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Quallent Pharmaceuticals Health LLC
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 82009-180
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 82009-181
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
REMEDYREPACK INC.
NDC Product
Human Prescription DrugDivalproex Sodium NDC 70518-3183
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 70518-3477
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rite Aid Corporation
NDC Product
Human Otc DrugFexofenadine Hydrochloride And Pseudoephedrine Hydrochloride NDC 11822-0021
- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rugby Laboratories
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
SpecGx LLC
NDC Product
Human Prescription DrugDextroamphetamine Sulfate Extended-release NDC 0406-8960
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Sulfate Extended-release NDC 0406-8961
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Sulfate Extended-release NDC 0406-8962
- Generic Name
- Dextroamphetamine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Strategic Sourcing Services, LLC
NDC Product
Human Otc DrugFexofenadine Hydrochloride And Pseudoephedrine Hydrochloride NDC 70677-1010
- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sun Pharmaceutical Industries, Inc.
NDC Product
Human Prescription DrugDapagliflozin And Metformin Hydrochloride NDC 63304-026
- Generic Name
- Dapagliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDapagliflozin And Metformin Hydrochloride NDC 63304-027
- Generic Name
- Dapagliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDapagliflozin And Metformin Hydrochloride NDC 63304-028
- Generic Name
- Dapagliflozin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
U.S. Pharmaceuticals
NDC Product
Human Prescription DrugDuavee NDC 63539-122
- Generic Name
- Conjugated Estrogens/bazedoxifene
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Unichem Pharmaceuticals (USA), Inc.
NDC Product
Human Prescription DrugAlfuzosin Hydrochloride NDC 29300-155
- Generic Name
- Alfuzosin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 29300-389
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 29300-399
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREEN CO.
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugPseudoephedrine Hydrochloride NDC 0363-6611
- Generic Name
- Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Wal-mart Stores, Inc.
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreens Company
NDC Product
Human Otc Drug- Generic Name
- Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Water-Jel Technologies
NDC Product
Human Otc DrugFirst Aid Antiseptic NDC 59898-401
- Generic Name
- Benzalkonium Chloride
- Dosage Form
- Spray
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Westminster Pharmaceuticals, LLC
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 69367-412
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 69367-413
- Generic Name
- Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
NDC Product
Human Prescription DrugDuavee NDC 0008-1123
- Generic Name
- Conjugated Estrogens/bazedoxifene
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Zydus Lifesciences Limited
NDC Product
Human Prescription DrugGabapentin NDC 70771-1861
- Generic Name
- Gabapentin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGabapentin NDC 70771-1862
- Generic Name
- Gabapentin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZituvimet Xr NDC 70771-1879
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZituvimet Xr NDC 70771-1880
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZituvimet Xr NDC 70771-1881
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSitagliptin And Metformin Hydrochloride NDC 70771-1886
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSitagliptin And Metformin Hydrochloride NDC 70771-1887
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSitagliptin And Metformin Hydrochloride NDC 70771-1888
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Zydus Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugGabapentin NDC 68382-607
- Generic Name
- Gabapentin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGabapentin NDC 68382-608
- Generic Name
- Gabapentin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugZituvimet Xr NDC 70710-1804
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZituvimet Xr NDC 70710-1805
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZituvimet Xr NDC 70710-1806
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSitagliptin And Metformin Hydrochloride NDC 70710-2036
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSitagliptin And Metformin Hydrochloride NDC 70710-2037
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSitagliptin And Metformin Hydrochloride NDC 70710-2038
- Generic Name
- Sitagliptin And Metformin Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
direct rx
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 72189-131
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
