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Data / Drug companies / Zhejiang Poly Pharm. Co., Ltd.

Zhejiang Poly Pharm. Co., Ltd.: 13 products in the FDA NDC directory, labeler code 72673

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

Zhejiang Poly Pharm. Co., Ltd. (labeler code 72673) lists 13 products in the FDA National Drug Code Directory, covering 6 finished drugs by generic name. By type: 13 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on February 21, 2026.

The request: Watch Zhejiang Poly Pharm. Co., Ltd. (FDA labeler code 72673): 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
72673
Products in commercial distribution
13
Packages
13
Finished drugs by generic name
6
Prescription products
13
Over the counter products
0
Controlled substance products
Schedule V 1
Flagged as original packager
13 of 13 products that carry the flag
Started marketing in the last 12 months
3
Earliest marketing start
February 6, 2023
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)13100%

Products by type

TypeProductsShare
Prescription drugs13100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Powder, for suspension646.2%
Capsule323.1%
Injection, solution323.1%
Solution17.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Brivaracetam72673-031SolutionGeneric drugs (ANDA)February 21, 2026
Oseltamivir phosphate72673-102CapsuleGeneric drugs (ANDA)December 31, 2025
Oseltamivir phosphate72673-101CapsuleGeneric drugs (ANDA)December 31, 2025
Voriconazole72673-111Powder, for suspensionGeneric drugs (ANDA)April 11, 2025
Azithromycin72673-084Powder, for suspensionGeneric drugs (ANDA)April 11, 2025
Azithromycin72673-083Powder, for suspensionGeneric drugs (ANDA)April 11, 2025
Azithromycin72673-082Powder, for suspensionGeneric drugs (ANDA)April 11, 2025
Azithromycin72673-081Powder, for suspensionGeneric drugs (ANDA)April 11, 2025
Fluconazole72673-091Powder, for suspensionGeneric drugs (ANDA)April 1, 2025
Oseltamivir phosphate72673-103CapsuleGeneric drugs (ANDA)November 29, 2023
Amiodarone Hydrochloride72673-073Injection, solutionGeneric drugs (ANDA)February 6, 2023
Amiodarone Hydrochloride72673-072Injection, solutionGeneric drugs (ANDA)February 6, 2023
Amiodarone Hydrochloride72673-071Injection, solutionGeneric drugs (ANDA)February 6, 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.