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Data / Drug companies / Northeast Pharma

Northeast Pharma: 7 products in the FDA NDC directory, labeler code 80136

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

Northeast Pharma (labeler code 80136) lists 7 products in the FDA National Drug Code Directory, covering 7 finished drugs by generic name. By type: 7 over the counter drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on September 26, 2023.

The request: Watch Northeast Pharma (FDA labeler code 80136): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
80136
Products in commercial distribution
7
Packages
8
Finished drugs by generic name
7
Prescription products
0
Over the counter products
7
Flagged as original packager
6 of 6 products that carry the flag
Started marketing in the last 12 months
0
Products with a marketing end date set
1
Earliest marketing start
January 22, 2021
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)342.9%
Over the counter monograph drugs228.6%
New drug applications (NDA)228.6%

Products by type

TypeProductsShare
Over the counter drugs7100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet342.9%
Tablet, delayed release114.3%
Capsule, liquid filled114.3%
Tablet, chewable114.3%
Capsule114.3%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Cetirizine HCl80136-856CapsuleNew drug applications (NDA)September 26, 2023
Gas Relief80136-859Tablet, chewableOver the counter monograph drugsJune 30, 2023
Loperamide Hydrochloride and Simethicone80136-384TabletGeneric drugs (ANDA)October 27, 2021
Nighttime Sleep-aid80136-785TabletOver the counter monograph drugsSeptember 1, 2021
Acid Reducer80136-852Tablet, delayed releaseGeneric drugs (ANDA)July 5, 2021
Anti-diarrheal80136-851Capsule, liquid filledNew drug applications (NDA)May 21, 2021
Anti-Diarrheal80136-063TabletGeneric drugs (ANDA)January 22, 2021

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.