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Data / Drug companies / Spi Pharma, Inc.

Spi Pharma, Inc.: 52 products in the FDA NDC directory, labeler code 12784

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

Spi Pharma, Inc. (labeler code 12784) lists 52 products in the FDA National Drug Code Directory. By type: 39 drugs for further processing, 13 bulk ingredients. Its main marketing category is drugs for further processing. The newest product started marketing on June 4, 2026.

The request: Watch Spi Pharma, Inc. (FDA labeler code 12784): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
12784
Products in commercial distribution
52
Packages
52
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
4
Earliest marketing start
November 12, 2012
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Drugs for further processing4994.2%
Bulk ingredients35.8%

Products by type

TypeProductsShare
Drugs for further processing3975%
Bulk ingredients1325%

Dosage forms

Dosage formProductsShare
Gel2038.5%
Powder1936.5%
Paste713.5%
Suspension47.7%
Liquid23.8%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Dried aluminum hydroxide gel12784-465GelDrugs for further processingJune 4, 2026
Aluminum hydroxide gel12784-134GelDrugs for further processingMarch 16, 2026
Aluminum hydroxide gel12784-464GelDrugs for further processingMarch 13, 2026
Magnesium hydroxide12784-463PasteDrugs for further processingMarch 13, 2026
Aluminum hydroxide12784-462GelBulk ingredientsMay 12, 2025
Aluminum hydroxide magnesium carbonate12784-460PowderDrugs for further processingSeptember 12, 2024
Aluminum hydroxide, magnesium carbonate12784-461PowderDrugs for further processingAugust 4, 2023
Aluminum hydroxide magnesium carbonate12784-460PowderDrugs for further processingJanuary 25, 2023
Aluminum, magnesium12784-432SuspensionDrugs for further processingJanuary 17, 2023
Magnesium hydroxide12784-459PowderDrugs for further processingSeptember 16, 2022
Magnesium hydroxide12784-458PowderDrugs for further processingMay 20, 2022
Magnesium hydroxide12784-192PowderDrugs for further processingJune 9, 2021
Magnesium hydroxide12784-456PowderDrugs for further processingMarch 19, 2021
Magaldrate12784-454GelDrugs for further processingMay 21, 2020
Aluminum magnesium sorbitol blend12784-452SuspensionDrugs for further processingJanuary 28, 2020
Aluminum hydroxide, magnesium carbonate12784-451PowderDrugs for further processingJanuary 28, 2020
Magnesium hydroxide12784-448PowderDrugs for further processingJanuary 28, 2020
Aluminum, magnesium12784-447LiquidDrugs for further processingJanuary 28, 2020
Aluminum, magnesium12784-430SuspensionDrugs for further processingJanuary 28, 2020
Aluminum, magnesium12784-446LiquidDrugs for further processingJanuary 27, 2020
Magnesium hydroxide12784-181PasteDrugs for further processingJanuary 27, 2020
Magnesium hydroxide12784-179PasteDrugs for further processingJanuary 27, 2020
Magnesium hydroxide12784-178PasteDrugs for further processingJanuary 27, 2020
Aluminum, magnesium12784-445SuspensionDrugs for further processingJanuary 24, 2020
Aluminum hydroxide12784-429GelDrugs for further processingJanuary 24, 2020

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.