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Data / Drug companies / Zhejiang Yongtai Pharmaceutical Co., Ltd

Zhejiang Yongtai Pharmaceutical Co., Ltd: 11 products in the FDA NDC directory, labeler code 69434

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

Zhejiang Yongtai Pharmaceutical Co., Ltd (labeler code 69434) lists 11 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 11 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on August 1, 2026.

The request: Watch Zhejiang Yongtai Pharmaceutical Co., Ltd (FDA labeler code 69434): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
69434
Products in commercial distribution
11
Packages
24
Finished drugs by generic name
4
Prescription products
11
Over the counter products
0
Flagged as original packager
11 of 11 products that carry the flag
Started marketing in the last 12 months
9
Earliest marketing start
January 9, 2025
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)11100%

Products by type

TypeProductsShare
Prescription drugs11100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Capsule545.5%
Tablet, film coated436.4%
Capsule, delayed release218.2%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Rosuvastatin Calcium69434-008Tablet, film coatedGeneric drugs (ANDA)August 1, 2026
Rosuvastatin Calcium69434-007Tablet, film coatedGeneric drugs (ANDA)August 1, 2026
Rosuvastatin Calcium69434-006Tablet, film coatedGeneric drugs (ANDA)August 1, 2026
Rosuvastatin Calcium69434-005Tablet, film coatedGeneric drugs (ANDA)August 1, 2026
Gabapentin69434-044CapsuleGeneric drugs (ANDA)July 1, 2026
Gabapentin69434-043CapsuleGeneric drugs (ANDA)July 1, 2026
Gabapentin69434-042CapsuleGeneric drugs (ANDA)July 1, 2026
Doxycycline Hyclate69434-017CapsuleGeneric drugs (ANDA)February 1, 2026
Doxycycline Hyclate69434-016CapsuleGeneric drugs (ANDA)February 1, 2026
Esomeprazole magnesium69434-013Capsule, delayed releaseGeneric drugs (ANDA)January 9, 2025
Esomeprazole magnesium69434-012Capsule, delayed releaseGeneric drugs (ANDA)January 9, 2025

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.