Skip to the page

Data / Drug companies / Mankind Pharma Limited

Mankind Pharma Limited: 13 products in the FDA NDC directory, labeler code 71231

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

Mankind Pharma Limited (labeler code 71231) lists 13 products in the FDA National Drug Code Directory. By type: 13 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on July 31, 2026.

The request: Watch Mankind Pharma Limited (FDA labeler code 71231): 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
71231
Products in commercial distribution
13
Packages
65
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
13
Earliest marketing start
June 24, 2026
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients13100%

Products by type

TypeProductsShare
Bulk ingredients13100%

Dosage forms

Dosage formProductsShare
Powder13100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Midodrine hydrochloride71231-135PowderBulk ingredientsJuly 31, 2026
Rocuronium bromide71231-133PowderBulk ingredientsJuly 31, 2026
Telmisartan71231-127PowderBulk ingredientsJuly 31, 2026
Rosuvastatin calcium71231-126PowderBulk ingredientsJuly 31, 2026
Rosuvastatin calcium71231-123PowderBulk ingredientsJuly 31, 2026
Nitrofurantoin monohydrate71231-139PowderBulk ingredientsJuly 22, 2026
Baclofen71231-138PowderBulk ingredientsJuly 22, 2026
Nitrofurantoin monohydrate71231-101PowderBulk ingredientsJuly 22, 2026
Baclofen71231-131PowderBulk ingredientsJuly 21, 2026
Propranolol hydrochloride71231-115PowderBulk ingredientsJuly 16, 2026
Propranolol hydrochloride71231-114PowderBulk ingredientsJuly 16, 2026
Nitrofurantoin macrocrystals71231-102PowderBulk ingredientsJuly 16, 2026
Succinylcholine-chloride71231-132PowderBulk ingredientsJune 24, 2026

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.