HYPROMELLOSE 2910 (15 MPA.S)
UNII 36SFW2JZ0W

Substance Identification & Data

This profile provides standardized clinical and technical data for Hypromellose 2910 (15 Mpa.s), uniquely identified by the FDA Unique Ingredient Identifier (UNII) 36SFW2JZ0W.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9004-65-3 and the RxNorm Concept ID (RxCUI) 1300450. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
36SFW2JZ0W
CAS Registry Number
9004-65-3
RxNorm Concept ID
1300450

Detailed Substance Profile

Preferred Name
HYPROMELLOSE 2910 (15 MPA.S)
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
36SFW2JZ0W
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 2910 (15 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

BENECEL HPMC E15
HPMC 2910 (15 CPS)
HYDROXYPROPYL METHYLCELLULOSE 2910 (15 CPS)
HYPROMELLOSE 2910 (15 CPS)
HYPROMELLOSE 2910 (15 MPA.S)
HYPROMELLOSE 2910 (15 MPA.S) [II]
HYPROMELLOSE E15

Brand / Trade Names

METHOCEL E15
METHOCEL E15LV
PHARMACOAT 615

NDC Products Containing HYPROMELLOSE 2910 (15 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 (500), only Active Listings are currently displayed. Display is limited to the first 200 products.
→ AbbVie Inc. 2
→ Actavis Pharma, Inc. 10
→ AiPing Pharmaceutical, Inc. 4
→ Ajanta Pharma USA Inc. 2
→ Amneal Pharmaceuticals of New York LLC 1
→ Apnar Pharma LP 2
→ AvKARE 2
→ Better Living Brands, LLC 1
→ Camber Pharmaceuticals, Inc. 24
→ Cosette Pharmaceuticals, Inc. 2
→ Cranbury Pharmaceuticals, LLC 1
→ Edenbridge Pharmaceuticals LLC. 1
→ Epic Pharma, LLC 1
→ HEB 2
→ HYVEE INC 2
→ Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. 10
→ Hikma Pharmaceuticals USA Inc 1
→ Hisun Pharmaceuticals USA Inc. 5
→ KROGER COMPANY 1
→ Lannett Company Inc. 1
→ Lannett Company, Inc. 1
→ Laurus Labs Limited 2
→ Macleods Pharmaceuticals Limited 2
→ Major Pharmaceuticals 5
→ Merck Sharp & Dohme LLC 6
→ Mylan Pharmaceuticals Inc. 4
→ NCS HealthCare of KY, LLC dba Vangard Labs 6
→ NorthStar Rx LLC 2
→ NorthStar RxLLC 2
→ PD-Rx Pharmaceuticals, Inc. 3
→ PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS 4
→ QPharma Inc 1
→ QPharma, Inc. 2
→ RUGBY LABORATORIES 1
→ Rising Pharma Holdings, Inc. 1
→ Rite Aid 5
→ Safeway, Inc 1
→ Sandoz Inc 5
→ TARGET CORPORATION 1
→ TOPCO ASSOCIATES LLC 1
→ TORRENT PHARMACEUTICALS LIMITED 4
→ Teva Pharmaceuticals USA, Inc. 22
→ Torrent Pharmaceuticals Limited 10
→ Unichem Pharmaceuticals (USA), Inc. 19
→ United Natural Foods, Inc. dba UNFI 1
→ Upsher-Smith Laboratories, LLC 1
→ Walgreens 3
→ Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. 10

AbbVie Inc.

NDC Product
Human Prescription Drug

Mavyret
NDC 0074-2600

Generic Name
Glecaprevir And Pibrentasvir
Dosage Form
Pellet
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Mavyret
NDC 0074-2625

Generic Name
Glecaprevir And Pibrentasvir
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing

Actavis Pharma, Inc.

NDC Product
Human Prescription Drug

Duloxetine
NDC 0228-2890

Generic Name
Duloxetine
Dosage Form
Capsule, Delayed Release Pellets
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0228-2890

Generic Name
Duloxetine
Dosage Form
Capsule, Delayed Release Pellets
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing

NDC 0228-2891

Generic Name
Duloxetine
Dosage Form
Capsule, Delayed Release Pellets
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Duloxetine
NDC 0228-2891

Generic Name
Duloxetine
Dosage Form
Capsule, Delayed Release Pellets
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Duloxetine
NDC 0228-2892

Generic Name
Duloxetine
Dosage Form
Capsule, Delayed Release Pellets
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0228-2892

Generic Name
Duloxetine
Dosage Form
Capsule, Delayed Release Pellets
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing

NDC 0591-0795

Generic Name
Dicyclomine Hydrochloride
Dosage Form
Tablet
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Dicyclomine Hydrochloride
NDC 0591-0795

Generic Name
Dicyclomine Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Bosentan
NDC 0591-2511

Generic Name
Bosentan
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Bosentan
NDC 0591-2512

Generic Name
Bosentan
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

AiPing Pharmaceutical, Inc.

NDC Product
Human Prescription Drug

Rosuvastatin
NDC 11788-130

Generic Name
Rosuvastatin
Dosage Form
Tablet, Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rosuvastatin
NDC 11788-131

Generic Name
Rosuvastatin
Dosage Form
Tablet, Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rosuvastatin
NDC 11788-132

Generic Name
Rosuvastatin
Dosage Form
Tablet, Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rosuvastatin
NDC 11788-133

Generic Name
Rosuvastatin
Dosage Form
Tablet, Coated
Route
Oral
Marketing
ANDA
Active Listing

Ajanta Pharma USA Inc.

NDC Product
Human Prescription Drug

Voriconazole
NDC 27241-062

Generic Name
Voriconazole
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Voriconazole
NDC 27241-063

Generic Name
Voriconazole
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Amneal Pharmaceuticals of New York LLC

NDC Product
Human Prescription Drug

Colesevelam Hydrochloride
NDC 0115-1320

Generic Name
Colesevelam Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Apnar Pharma LP

NDC Product
Human Prescription Drug

Bupropion Hydrochloride
NDC 24689-119

Generic Name
Bupropion Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Bupropion Hydrochloride
NDC 24689-120

Generic Name
Bupropion Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

AvKARE

NDC Product
Human Prescription Drug

Azithromycin
NDC 42291-044

Generic Name
Azithromycin
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Primaquine Phosphate
NDC 42291-510

Generic Name
Primaquine Phosphate
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Better Living Brands, LLC

NDC Product
Human Otc Drug

Ibuprofen And Diphenhydramine Citrate
NDC 21130-228

Generic Name
Ibuprofen And Diphenhydramine Citrate
Dosage Form
Tablet, Coated
Route
Oral
Marketing
ANDA
Active Listing

Camber Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Famotidine
NDC 31722-017

Generic Name
Famotidine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Famotidine
NDC 31722-018

Generic Name
Famotidine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nitazoxanide
NDC 31722-100

Generic Name
Nitazoxanide
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Cinacalcet
NDC 31722-103

Generic Name
Cinacalcet
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Cinacalcet
NDC 31722-104

Generic Name
Cinacalcet
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Cinacalcet
NDC 31722-105

Generic Name
Cinacalcet
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Prucalopride
NDC 31722-391

Generic Name
Prucalopride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Prucalopride
NDC 31722-392

Generic Name
Prucalopride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Eletriptan Hydrobromide
NDC 31722-443

Generic Name
Eletriptan Hydrobromide
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Eletriptan Hydrobromide
NDC 31722-444

Generic Name
Eletriptan Hydrobromide
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Lopinavir And Ritonavir
NDC 31722-556

Generic Name
Lopinavir And Ritonavir
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Lopinavir And Ritonavir
NDC 31722-603

Generic Name
Lopinavir And Ritonavir
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tadalafil
NDC 31722-643

Generic Name
Tadalafil
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tadalafil
NDC 31722-644

Generic Name
Tadalafil
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tadalafil
NDC 31722-645

Generic Name
Tadalafil
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tadalafil
NDC 31722-646

Generic Name
Tadalafil
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tadalafil
NDC 31722-647

Generic Name
Tadalafil
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Sacubitril And Valsartan
NDC 31722-673

Generic Name
Sacubitril And Valsartan
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Sacubitril And Valsartan
NDC 31722-674

Generic Name
Sacubitril And Valsartan
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Sacubitril And Valsartan
NDC 31722-675

Generic Name
Sacubitril And Valsartan
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Varenicline
NDC 31722-678

Generic Name
Varenicline Tartrate
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Varenicline
NDC 31722-679

Generic Name
Varenicline Tartrate
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Varenicline
NDC 31722-690

Generic Name
Varenicline Tartrate
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing

Cosette Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Effient
NDC 0713-0881

Generic Name
Prasugrel Hydrochloride
Dosage Form
Tablet, Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Effient
NDC 0713-0882

Generic Name
Prasugrel Hydrochloride
Dosage Form
Tablet, Coated
Route
Oral
Marketing
NDA
Active Listing

Cranbury Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Colesevelam Hydrochloride
NDC 27808-190

Generic Name
Colesevelam Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Edenbridge Pharmaceuticals LLC.

NDC Product
Human Prescription Drug

Vigabatrin
NDC 42799-950

Generic Name
Vigabatrin
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Epic Pharma, LLC

NDC Product
Human Prescription Drug

Benzphetamine Hydrochloride
NDC 42806-081

Generic Name
Benzphetamine Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

HEB

NDC Product
Human Otc Drug

Allergy Relief
NDC 37808-391

Generic Name
Fexofenadine Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Allergy Relief
NDC 37808-392

Generic Name
Fexofenadine Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

HYVEE INC

NDC Product
Human Otc Drug

Allergy Relief
NDC 42507-192

Generic Name
Fexofenadine Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Mucus Relief
NDC 42507-253

Generic Name
Guaifenesin
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Glipizide And Metformin Hcl
NDC 23155-115

Generic Name
Glipizide And Metformin Hcl
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Glipizide And Metformin Hcl
NDC 23155-116

Generic Name
Glipizide And Metformin Hcl
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Glipizide And Metformin Hcl
NDC 23155-117

Generic Name
Glipizide And Metformin Hcl
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Doxycycline
NDC 23155-133

Generic Name
Doxycycline
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Doxycycline
NDC 23155-134

Generic Name
Doxycycline
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Doxycycline
NDC 23155-135

Generic Name
Doxycycline
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Doxycycline
NDC 23155-136

Generic Name
Doxycycline
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Glyburide-metformin Hydrochloride
NDC 23155-233

Generic Name
Glyburide-metformin Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Glyburide-metformin Hydrochloride
NDC 23155-234

Generic Name
Glyburide-metformin Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Glyburide-metformin Hydrochloride
NDC 23155-235

Generic Name
Glyburide-metformin Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Hikma Pharmaceuticals USA Inc

NDC Product
Human Prescription Drug

Combogesic
NDC 0143-9432

Generic Name
Acetaminophen And Ibuprofen
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing

Hisun Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Irbesartan
NDC 42658-121

Generic Name
Irbesartan
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Irbesartan
NDC 42658-122

Generic Name
Irbesartan
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Irbesartan
NDC 42658-123

Generic Name
Irbesartan
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Irbesartan And Hydrochlorothiazide
NDC 42658-141

Generic Name
Irbesartan And Hydrochlorothiazide
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Irbesartan And Hydrochlorothiazide
NDC 42658-142

Generic Name
Irbesartan And Hydrochlorothiazide
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

KROGER COMPANY

NDC Product
Human Otc Drug

Ibuprofen Pm
NDC 30142-278

Generic Name
Ibuprofen And Diphenhydramine Citrate
Dosage Form
Tablet, Coated
Route
Oral
Marketing
ANDA
Active Listing

Lannett Company Inc.

NDC Product
Human Prescription Drug

Mesalamine
NDC 0527-3012

Generic Name
Mesalamine
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Lannett Company, Inc.

NDC Product
Human Prescription Drug

Fluvastatin Sodium
NDC 0527-2580

Generic Name
Fluvastatin Sodium
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Laurus Labs Limited

NDC Product
Human Prescription Drug

Lopinavir And Ritonavir
NDC 42385-933

Generic Name
Lopinavir And Ritonavir
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Lopinavir And Ritonavir
NDC 42385-934

Generic Name
Lopinavir And Ritonavir
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Macleods Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Irbesartan And Hydrochlorothiazide
NDC 33342-057

Generic Name
Irbesartan And Hydrochlorothiazide
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Irbesartan And Hydrochlorothiazide
NDC 33342-058

Generic Name
Irbesartan And Hydrochlorothiazide
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Major Pharmaceuticals

NDC Product
Human Prescription Drug

Clarithromycin
NDC 0904-6872

Generic Name
Clarithromycin
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Voriconazole
NDC 0904-7024

Generic Name
Voriconazole
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Azithromycin
NDC 0904-7350

Generic Name
Azithromycin
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Azithromycin
NDC 0904-7351

Generic Name
Azithromycin
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Merck Sharp & Dohme LLC

NDC Product
Human Prescription Drug

Zepatier
NDC 0006-3074

Generic Name
Elbasvir And Grazoprevir
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Prevymis
NDC 0006-3075

Generic Name
Letermovir
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Prevymis
NDC 0006-3076

Generic Name
Letermovir
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Prevymis
NDC 0006-5003

Generic Name
Letermovir
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Prevymis
NDC 0006-5004

Generic Name
Letermovir
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Idvynso
NDC 0006-5092

Generic Name
Doravirine, Islatravir
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing

Mylan Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Buprenorphine And Naloxone
NDC 0378-8765

Generic Name
Buprenorphine And Naloxone
Dosage Form
Film
Route
Buccal; Sublingual
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Buprenorphine And Naloxone
NDC 0378-8766

Generic Name
Buprenorphine And Naloxone
Dosage Form
Film
Route
Buccal; Sublingual
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Buprenorphine And Naloxone
NDC 0378-8767

Generic Name
Buprenorphine And Naloxone
Dosage Form
Film
Route
Buccal; Sublingual
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Buprenorphine And Naloxone
NDC 0378-8768

Generic Name
Buprenorphine And Naloxone
Dosage Form
Film
Route
Buccal; Sublingual
Marketing
ANDA
Active Listing

NCS HealthCare of KY, LLC dba Vangard Labs

NDC Product
Human Prescription Drug

Cyclobenzaprine Hydrochloride
NDC 0615-8508

Generic Name
Cyclobenzaprine Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rosuvastatin Calcium
NDC 0615-8532

Generic Name
Rosuvastatin Calcium
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rosuvastatin Calcium
NDC 0615-8533

Generic Name
Rosuvastatin Calcium
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rosuvastatin Calcium
NDC 0615-8534

Generic Name
Rosuvastatin Calcium
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rosuvastatin Calcium
NDC 0615-8535

Generic Name
Rosuvastatin Calcium
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dicyclomine Hydrochloride
NDC 0615-8622

Generic Name
Dicyclomine Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

NorthStar Rx LLC

NDC Product
Human Prescription Drug

Lansoprazole
NDC 16714-185

Generic Name
Lansoprazole
Dosage Form
Tablet, Orally Disintegrating, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Lansoprazole
NDC 16714-186

Generic Name
Lansoprazole
Dosage Form
Tablet, Orally Disintegrating, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

NorthStar RxLLC

NDC Product
Human Prescription Drug

Entecavir
NDC 16714-717

Generic Name
Entecavir
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Entecavir
NDC 16714-718

Generic Name
Entecavir
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

PD-Rx Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Dicyclomine Hydrochloride
NDC 43063-045

Generic Name
Dicyclomine Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Clarithromycin
NDC 43063-823

Generic Name
Clarithromycin
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Potassium
NDC 43063-848

Generic Name
Diclofenac Potassium
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS

NDC Product
Human Prescription Drug

Rosuvastatin Calcium
NDC 24658-261

Generic Name
Rosuvastatin Calcium
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rosuvastatin Calcium
NDC 24658-262

Generic Name
Rosuvastatin Calcium
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rosuvastatin Calcium
NDC 24658-263

Generic Name
Rosuvastatin Calcium
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rosuvastatin Calcium
NDC 24658-264

Generic Name
Rosuvastatin Calcium
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

QPharma Inc

NDC Product
Human Prescription Drug

Omeprazole
NDC 42708-170

Generic Name
Omeprazole
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

QPharma, Inc.

NDC Product
Human Prescription Drug

Amoxicillin
NDC 42708-078

Generic Name
Amoxicillin
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Amoxicillin
NDC 42708-112

Generic Name
Amoxicillin
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

RUGBY LABORATORIES

NDC Product
Human Otc Drug

Acetaminophen And Ibuprofen
NDC 0536-1376

Generic Name
Acetaminophen And Ibuprofen
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Rising Pharma Holdings, Inc.

NDC Product
Human Prescription Drug

Dicyclomine Hydrochloride
NDC 16571-259

Generic Name
Dicyclomine Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Rite Aid

NDC Product
Human Otc Drug

Fexofenadine Hcl
NDC 11822-7652

Generic Name
Fexofenadine Hcl
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Fexofenadine Hcl
NDC 11822-7660

Generic Name
Fexofenadine Hcl
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Fexofenadine Hcl
NDC 11822-7661

Generic Name
Fexofenadine Hcl
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Fexofenadine Hcl
NDC 11822-7663

Generic Name
Fexofenadine Hcl
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Fexofenadine Hcl
NDC 11822-7664

Generic Name
Fexofenadine Hcl
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Safeway, Inc

NDC Product
Human Otc Drug

Fexofenadine Hcl
NDC 21130-769

Generic Name
Fexofenadine Hcl
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Sandoz Inc

NDC Product
Human Prescription Drug

Omeprazole
NDC 0781-2859

Generic Name
Omeprazole
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Omeprazole
NDC 0781-2868

Generic Name
Omeprazole
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Zolpidem Tartrate
NDC 0781-5317

Generic Name
Zolpidem Tartrate
Dosage Form
Tablet, Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Zolpidem Tartrate
NDC 0781-5318

Generic Name
Zolpidem Tartrate
Dosage Form
Tablet, Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Ezetimibe
NDC 0781-5690

Generic Name
Ezetimibe
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

TARGET CORPORATION

NDC Product
Human Otc Drug

Fexofenadine Hcl
NDC 11673-767

Generic Name
Fexofenadine Hcl
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

TOPCO ASSOCIATES LLC

NDC Product
Human Otc Drug

Allergy Relief
NDC 36800-653

Generic Name
Fexofenadine Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

TORRENT PHARMACEUTICALS LIMITED

NDC Product
Human Prescription Drug

Rosuvastatin Calcium
NDC 13668-720

Generic Name
Rosuvastatin Calcium
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rosuvastatin Calcium
NDC 13668-721

Generic Name
Rosuvastatin Calcium
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rosuvastatin Calcium
NDC 13668-722

Generic Name
Rosuvastatin Calcium
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rosuvastatin Calcium
NDC 13668-723

Generic Name
Rosuvastatin Calcium
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Tolterodine Tartrate
NDC 0093-0010

Generic Name
Tolterodine Tartrate
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Moexipril Hydrochloride
NDC 0093-0017

Generic Name
Moexipril Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tolterodine Tartrate
NDC 0093-0018

Generic Name
Tolterodine Tartrate
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Potassium
NDC 0093-0948

Generic Name
Diclofenac Potassium
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Etodolac
NDC 0093-1118

Generic Name
Etodolac
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Etodolac
NDC 0093-1122

Generic Name
Etodolac
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Quetiapine
NDC 0093-2063

Generic Name
Quetiapine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Camrese
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 Drug

Estradiol
NDC 0093-3223

Generic Name
Estradiol
Dosage Form
Insert
Route
Vaginal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tramadol Hydrochloride
NDC 0093-3301

Generic Name
Tramadol Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Moexipril Hydrochloride
NDC 0093-5150

Generic Name
Moexipril Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Camrese Lo
NDC 0093-6148

Generic Name
Levonorgestrel/ethinyl Estradiol And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Etodolac
NDC 0093-7172

Generic Name
Etodolac
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Raloxifene Hydrochloride
NDC 0093-7290

Generic Name
Raloxifene Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Clopidogrel
NDC 0093-7314

Generic Name
Clopidogrel
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Quetiapine
NDC 0093-8162

Generic Name
Quetiapine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Quetiapine
NDC 0093-8163

Generic Name
Quetiapine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Quetiapine
NDC 0093-8164

Generic Name
Quetiapine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Quetiapine
NDC 0093-8165

Generic Name
Quetiapine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Quetiapine
NDC 0093-8166

Generic Name
Quetiapine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diflunisal
NDC 0093-9222

Generic Name
Diflunisal
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Aviane
NDC 0555-9045

Generic Name
Levonorgestrel And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing

Torrent Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Darifenacin
NDC 13668-202

Generic Name
Darifenacin
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Darifenacin
NDC 13668-203

Generic Name
Darifenacin
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Carbamazepine
NDC 13668-284

Generic Name
Carbamazepine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Carbamazepine
NDC 13668-285

Generic Name
Carbamazepine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Carbamazepine
NDC 13668-286

Generic Name
Carbamazepine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tadalafil
NDC 13668-565

Generic Name
Tadalafil
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tadalafil
NDC 13668-566

Generic Name
Tadalafil
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tadalafil
NDC 13668-567

Generic Name
Tadalafil
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tadalafil
NDC 13668-568

Generic Name
Tadalafil
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tadalafil
NDC 13668-581

Generic Name
Tadalafil
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Unichem Pharmaceuticals (USA), Inc.

NDC Product
Human Prescription Drug

Losartan Potassium
NDC 29300-144

Generic Name
Losartan Potassium
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Losartan Potassium
NDC 29300-145

Generic Name
Losartan Potassium
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Losartan Potassium
NDC 29300-146

Generic Name
Losartan Potassium
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Losartan Potassium And Hydrochlorothiazide
NDC 29300-190

Generic Name
Losartan Potassium And Hydrochlorothiazide
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Losartan Potassium And Hydrochlorothiazide
NDC 29300-191

Generic Name
Losartan Potassium And Hydrochlorothiazide
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Losartan Potassium And Hydrochlorothiazide
NDC 29300-192

Generic Name
Losartan Potassium And Hydrochlorothiazide
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Quetiapine
NDC 29300-309

Generic Name
Quetiapine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Quetiapine
NDC 29300-310

Generic Name
Quetiapine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Quetiapine
NDC 29300-311

Generic Name
Quetiapine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Quetiapine
NDC 29300-312

Generic Name
Quetiapine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nebivolol Hydrochloride
NDC 29300-375

Generic Name
Nebivolol Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nebivolol Hydrochloride
NDC 29300-376

Generic Name
Nebivolol Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nebivolol Hydrochloride
NDC 29300-377

Generic Name
Nebivolol Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nebivolol Hydrochloride
NDC 29300-378

Generic Name
Nebivolol Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 29300-380

Generic Name
Divalproex Sodium
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 29300-381

Generic Name
Divalproex Sodium
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Cyclobenzaprine Hydrochloride
NDC 29300-413

Generic Name
Cyclobenzaprine Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Cyclobenzaprine Hydrochloride
NDC 29300-414

Generic Name
Cyclobenzaprine Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Cyclobenzaprine Hydrochloride
NDC 29300-415

Generic Name
Cyclobenzaprine Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

United Natural Foods, Inc. dba UNFI

NDC Product
Human Otc Drug

Allergy Relief
NDC 41163-292

Generic Name
Fexofenadine Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Upsher-Smith Laboratories, LLC

NDC Product
Human Prescription Drug

Dicyclomine Hydrochloride
NDC 24979-200

Generic Name
Dicyclomine Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Walgreens

NDC Product
Human Otc Drug

Omeprazole
NDC 0363-9510

Generic Name
Omeprazole
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Fexofenadine Hcl
NDC 0363-9760

Generic Name
Fexofenadine Hcl
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Fexofenadine Hcl
NDC 0363-9765

Generic Name
Fexofenadine Hcl
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.

NDC Product
Human Prescription Drug

Premarin
NDC 0046-1100

Generic Name
Estrogens, Conjugated
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Premarin
NDC 0046-1101

Generic Name
Estrogens, Conjugated
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Premarin
NDC 0046-1102

Generic Name
Estrogens, Conjugated
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Premarin
NDC 0046-1103

Generic Name
Estrogens, Conjugated
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Premarin
NDC 0046-1104

Generic Name
Estrogens, Conjugated
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Prempro
NDC 0046-1105

Generic Name
Conjugated Estrogens And Medroxyprogesterone Acetate
Dosage Form
Tablet, Sugar Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Prempro
NDC 0046-1106

Generic Name
Conjugated Estrogens And Medroxyprogesterone Acetate
Dosage Form
Tablet, Sugar Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Prempro
NDC 0046-1107

Generic Name
Conjugated Estrogens And Medroxyprogesterone Acetate
Dosage Form
Tablet, Sugar Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Prempro
NDC 0046-1108

Generic Name
Conjugated Estrogens And Medroxyprogesterone Acetate
Dosage Form
Tablet, Sugar Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Premphase
NDC 0046-2575

Generic Name
Conjugated Estrogens And Medroxyprogesterone Acetate
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing

External Clinical & Regulatory Resources

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