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Data / Drug companies / Rising Pharma Holdings, Inc.

Rising Pharma Holdings, Inc.: 165 products in the FDA NDC directory, labeler code 57237

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Rising Pharma Holdings, Inc. (labeler code 57237) lists 165 products in the FDA National Drug Code Directory, covering 66 finished drugs by generic name. By type: 121 prescription drugs, 44 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on October 10, 2026.

The request: Watch Rising Pharma Holdings, Inc. (FDA labeler code 57237): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
57237
Products in commercial distribution
165
Packages
317
Finished drugs by generic name
66
Prescription products
121
Over the counter products
44
Controlled substance products
Schedule IV 4
Flagged as original packager
149 of 149 products that carry the flag
Started marketing in the last 12 months
11
Products with a marketing end date set
2
Earliest marketing start
October 22, 2004
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)12777%
Over the counter monograph drugs3521.2%
Other unapproved drugs31.8%

Products by type

TypeProductsShare
Prescription drugs12173.3%
Over the counter drugs4426.7%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Mirtazapine742
Fluconazole648
Amoxicillin635
Pramipexole dihydrochloride623
Amlodipine and benazepril hydrochloride614
Venlafaxine hydrochloride548
Cefprozil47
Rosuvastatin calcium434
Nicotine polacrilex457
Rizatriptan benzoate425
Torsemide425
Glycerin456
Ramipril419
Glyburide and metformin hydrochloride39
Cefadroxil315
Diphenhydramine hydrochloride3127
Sennosides365
Trandolapril35
Omeprazole3106
Acetaminophen3214
Metoprolol tartrate346
Repaglinide39
Pioglitazone317
Divalproex sodium348
Flecainide acetate313
Felodipine315
Galantamine38
Montelukast sodium331
Penicillin v potassium218
Clarithromycin227
Cefuroxime axetil217
Ondansetron252
Cetirizine hydrochloride2119
Pioglitazone hydrochloride and metformin hydrochloride22
Zaleplon210
Dextromethorphan hbr. and guaifenesin22
Aluminum hydroxide, magnesium hydroxide, and simethicone26
Phenazopyridine hydrochloride253
Bisacodyl260
Aspirin2134
Valacyclovir hydrochloride228
Finasteride231
Sulfamethoxazole and trimethoprim248
Diphenhydramine hcl oral22
Ondansetron hydrochloride248
Modafinil225
Tolnaftate199
Magnesium hydroxide141
Clotrimazole antifungal11
Lidocaine 5%123
Cefdinir125
Camphor, menthol, methyl salicylate136
Trolamine salicylate 10%13
Meclizine hydrochloride141
Guaifenesin1123
Sodium chloride171
Alfuzosin hydrochloride113
Moxifloxacin hydrochloride120
Methenamine, sodium salicylate117
Lamivudine114
Lansoprazole, amoxicillin, clarithromycin11
Hydrochlorothiazide151
Acetaminophen, aspirin and caffeine126
Diphenhydramine hydrochloride and zinc acetate112
Guaifenesin, dextromethorphan hbr126
Tamsulosin hydrochloride138

Dosage forms

Dosage formProductsShare
Tablet4426.7%
Tablet, film coated4024.2%
Capsule1810.9%
Powder, for suspension84.8%
Solution84.8%
Tablet, orally disintegrating74.2%
Cream63.6%
Liquid53%
Suppository53%
Tablet, delayed release42.4%
Tablet, film coated, extended release42.4%
Capsule, delayed release31.8%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Proctozone-B57237-372Tablet, coatedOver the counter monograph drugsOctober 10, 2026
Senaklear57237-371Tablet, film coatedOver the counter monograph drugsSeptember 30, 2026
Dimetane57237-368Capsule, liquid filledOver the counter monograph drugsJanuary 27, 2026
Dimetane57237-367Capsule, liquid filledOver the counter monograph drugsJanuary 27, 2026
Mucolyte DM57237-360LiquidOver the counter monograph drugsDecember 22, 2025
Mucolyte57237-359LiquidOver the counter monograph drugsDecember 22, 2025
Lidonumb57237-353CreamOver the counter monograph drugsDecember 18, 2025
Jointiva57237-355CreamOver the counter monograph drugsDecember 16, 2025
Pedikleer57237-354CreamOver the counter monograph drugsDecember 16, 2025
Cetirizine hydrochloride57237-358SolutionGeneric drugs (ANDA)November 11, 2025
Cetirizine hydrochloride57237-357SolutionGeneric drugs (ANDA)November 11, 2025
Sodium Chloride57237-361TabletOver the counter monograph drugsNovember 6, 2025
ItchZap57237-352CreamOver the counter monograph drugsNovember 6, 2025
Coolexa57237-351CreamOver the counter monograph drugsNovember 6, 2025
Micoclear57237-350CreamOver the counter monograph drugsNovember 6, 2025
Proctozone GMax57237-339SuppositoryOver the counter monograph drugsJuly 31, 2025
Proctozone-G57237-338SuppositoryOver the counter monograph drugsJuly 31, 2025
Adult Low Dose Aspirin57237-349Tablet, delayed releaseOver the counter monograph drugsJuly 9, 2025
Acetaminophen, Aspirin and Caffeine57237-348TabletOver the counter monograph drugsJuly 9, 2025
Acetaminophen57237-347Tablet, film coatedOver the counter monograph drugsJuly 9, 2025
Acetaminophen57237-346Tablet, film coatedOver the counter monograph drugsJuly 9, 2025
Proctozone-B57237-337SuppositoryOver the counter monograph drugsDecember 1, 2024
Meclizine HCl57237-333TabletOver the counter monograph drugsJuly 22, 2024
Diphenhydramine HCl Oral Solution57237-318SolutionOver the counter monograph drugsDecember 15, 2023
Diphenhydramine HCl Oral Solution57237-317SolutionOver the counter monograph drugsDecember 15, 2023

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.