Shandong Xinhua Pharmaceutical
NDC Database
Shandong Xinhua Pharmaceutical
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 43
- Latest Marketing Date 2026-01-19
- Data Source FDA
- First Marketing Date 1983-10-01
Company Overview
Company
Shandong Xinhua Pharmaceutical
Country
China
Website
Social Profiles
Company Snapshot
Shandong Xinhua Pharmaceutical
No. 1 Lutai Avenue, Zibo High-tech Zone, Shandong Province
China
xhzy.com/html/english/default.aspx pengxinwen@xhzy.com View on MapNDC Records ( 43 records )
Nonproprietary Name
Carbidopa
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Co Ltd
Marketing Category
BULK INGREDIENT
Substance
CARBIDOPA
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1984-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Aspirin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Co Ltd
Marketing Category
BULK INGREDIENT
Substance
ASPIRIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1985-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Aspirin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Co Ltd
Marketing Category
BULK INGREDIENT
Substance
ASPIRIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1985-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Aspirin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Co Ltd
Marketing Category
BULK INGREDIENT
Substance
ASPIRIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1985-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Aspirin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Co Ltd
Marketing Category
BULK INGREDIENT
Substance
ASPIRIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1985-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Aspirin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Co Ltd
Marketing Category
BULK INGREDIENT
Substance
ASPIRIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1985-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
IBUPROFEN
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
IBUPROFEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1987-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ibuprofen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
IBUPROFEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1987-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Calcium Polycarbophil
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
CALCIUM POLYCARBOPHIL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1990-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
TRAMADOL HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
TRAMADOL HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CIV
Start Marketing Date
2003-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
LEVODOPA
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
LEVODOPA
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2000-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Levodopa
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
LEVODOPA
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2000-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Caffeine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
CAFFEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1987-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Caffeine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
CAFFEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1987-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
CAFFEINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
CAFFEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1987-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
CAFFEINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
CAFFEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1987-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Caffeine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
CAFFEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1987-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
CAFFEINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
CAFFEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1987-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Caffeine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
CAFFEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1987-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Caffeine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
CAFFEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1987-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Theophylline
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
THEOPHYLLINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1998-08-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Meloxicam
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
MELOXICAM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2007-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Aspirin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
ASPIRIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1985-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Aspirin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
ASPIRIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1985-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Aspirin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
ASPIRIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1985-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Aspirin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
ASPIRIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1985-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Aspirin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
ASPIRIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1985-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Nimodipine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
NIMODIPINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2008-04-07
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Aspirin
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
ASPIRIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1985-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Phenobarbital
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
PHENOBARBITAL
Product Type
BULK INGREDIENT
DEA Schedule
CIV
Start Marketing Date
1997-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Caffeine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
CAFFEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1987-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ibuprofen Sodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
IBUPROFEN SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-06-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
AMINOPHYLLINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
AMINOPHYLLINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1983-10-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
SALICYLIC ACID
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
SALICYLIC ACID
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1994-06-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ASPIRIN
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
ASPIRIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1985-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Hydrocortisone
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
HYDROCORTISONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1984-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Hydrocortisone
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
HYDROCORTISONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1984-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Hydrocortisone
Dosage Form
POULTICE
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
HYDROCORTISONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1984-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Hydrocortisone
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
HYDROCORTISONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1984-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Hydrocortisone Acetate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
HYDROCORTISONE ACETATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1984-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Hydrocortisone Acetate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
HYDROCORTISONE ACETATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1984-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Hydrocortisone Acetate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
HYDROCORTISONE ACETATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1984-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Theophylline Anhydrous
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
Shandong Xinhua Pharmaceutical Company Limited
Marketing Category
BULK INGREDIENT
Substance
THEOPHYLLINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2026-01-19
End Marketing Date
-
Listing Record Certified Through
2027-12-31
NDC Type Breakdown
43 total- Bulk Ingredient
Official Source
NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).
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NDC
58624-0621
Nonproprietary Name
Carbidopa
Labeler
Shandong Xinhua Pharmaceutical Co Ltd
Dosage Form
POWDER
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