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Data / Drug companies / Shandong New Time Pharmaceutical Co., Ltd.

Shandong New Time Pharmaceutical Co., Ltd.: 31 products in the FDA NDC directory, labeler code 42677

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

Shandong New Time Pharmaceutical Co., Ltd. (labeler code 42677) lists 31 products in the FDA National Drug Code Directory, covering 9 finished drugs by generic name. By type: 22 prescription drugs, 5 bulk ingredients. Its main marketing category is generic drugs (ANDA). The newest product started marketing on April 17, 2026.

The request: Watch Shandong New Time Pharmaceutical Co., Ltd. (FDA labeler code 42677): 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
42677
Products in commercial distribution
31
Packages
37
Finished drugs by generic name
9
Prescription products
22
Over the counter products
0
Flagged as original packager
20 of 20 products that carry the flag
Started marketing in the last 12 months
4
Earliest marketing start
November 21, 2006
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)2271%
Bulk ingredients412.9%
Drugs for further processing412.9%
Bulk ingredients for compounding13.2%

Products by type

TypeProductsShare
Prescription drugs2271%
Bulk ingredients516.1%
Drugs for further processing412.9%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Injection, solution929%
Powder722.6%
Liquid516.1%
Tablet, film coated412.9%
Capsule39.7%
Tablet, extended release39.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Rosuvastatin Calcium42677-304Tablet, film coatedGeneric drugs (ANDA)April 17, 2026
Rosuvastatin Calcium42677-303Tablet, film coatedGeneric drugs (ANDA)April 17, 2026
Oxaliplatin42677-337Injection, solutionGeneric drugs (ANDA)January 15, 2026
Oxaliplatin42677-336Injection, solutionGeneric drugs (ANDA)January 15, 2026
Isoflurane42677-327LiquidGeneric drugs (ANDA)November 4, 2025
Isoflurane42677-326LiquidGeneric drugs (ANDA)November 4, 2025
Oseltamivir phosphate42677-322CapsuleGeneric drugs (ANDA)July 9, 2025
Oseltamivir phosphate42677-321CapsuleGeneric drugs (ANDA)July 9, 2025
Oseltamivir phosphate42677-320CapsuleGeneric drugs (ANDA)July 9, 2025
Milrinone Lactate42677-338Injection, solutionGeneric drugs (ANDA)June 5, 2025
Sugammadex42677-312Injection, solutionGeneric drugs (ANDA)May 1, 2025
Sugammadex42677-311Injection, solutionGeneric drugs (ANDA)May 1, 2025
Milrinone42677-107PowderBulk ingredientsMarch 24, 2025
Rocuronium Bromide42677-310Injection, solutionGeneric drugs (ANDA)July 12, 2024
Rocuronium Bromide42677-309Injection, solutionGeneric drugs (ANDA)July 12, 2024
Isosorbide Mononitrate42677-306Tablet, extended releaseGeneric drugs (ANDA)February 8, 2024
Isosorbide Mononitrate42677-305Tablet, extended releaseGeneric drugs (ANDA)February 8, 2024
Sevoflurane42677-308LiquidGeneric drugs (ANDA)August 18, 2023
Milrinone Lactate42677-314Injection, solutionGeneric drugs (ANDA)January 23, 2023
Milrinone Lactate42677-313Injection, solutionGeneric drugs (ANDA)January 23, 2023
Isosorbide Mononitrate42677-307Tablet, extended releaseGeneric drugs (ANDA)April 29, 2022
Orlistat42677-119PowderBulk ingredientsApril 1, 2022
Rosuvastatin Calcium42677-302Tablet, film coatedGeneric drugs (ANDA)January 22, 2022
Rosuvastatin Calcium42677-301Tablet, film coatedGeneric drugs (ANDA)January 22, 2022
Isoflurane42677-114LiquidBulk ingredientsJanuary 1, 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.