National Drug Code (NDC) Database
Shenzhen Hepalink Pharmaceutical Group Co.,Ltd.
-
NDC:
67957-0002
-
Nonproprietary Name:
Heparin Sodium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
HEPARIN SODIUM
-
Start Marketing Date:
2020-09-04
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Shenzhen Mengyue Technology Co., Ltd.
-
NDC:
87255-010
-
Nonproprietary Name:
CHICKEN DEWORMER
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
10; 10; 4; 3; 10; 3; 8; 2 g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g
-
Substance:
BLACK PEPPER; CAPSICUM; CHITIN; FLAX SEED; GARLIC; OREGANO; OYSTER SHELL CALCIUM CARBONATE, CRUDE; VITAMIN A
-
Start Marketing Date:
2026-05-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Shenzhen Oriental Pharmaceutical Co. Ltd
-
NDC:
64431-0003
-
Nonproprietary Name:
Doxylamine Succinate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DOXYLAMINE SUCCINATE
-
Start Marketing Date:
2015-08-05
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Shenzhen Oriental Pharmaceutical Co. Ltd.
-
NDC:
64431-0001
-
Nonproprietary Name:
Phenylephrine Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
PHENYLEPHRINE HYDROCHLORIDE
-
Start Marketing Date:
2016-09-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Shenzhen Oriental Pharmaceutical Co., Ltd.
-
NDC:
64431-0004
-
Nonproprietary Name:
Phenylephrine Bitartrate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
PHENYLEPHRINE BITARTRATE
-
Start Marketing Date:
2016-10-19
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Shenzhen Techdow Pharmaceutical Co., Ltd.
-
NDC:
19657-0003
-
Nonproprietary Name:
Enoxaparin Sodium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ENOXAPARIN SODIUM
-
Start Marketing Date:
2018-10-10
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Shenzhou Jiheng Pharmaceutical Co., Ltd.
-
NDC:
82097-0909
-
Nonproprietary Name:
acetaminophen
-
Dosage Form:
GRANULE
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ACETAMINOPHEN
-
Start Marketing Date:
2024-10-26
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Shield Pharmaceuticals Corp
-
NDC:
83059-0161
-
Nonproprietary Name:
ACETAMINOPHEN
-
Dosage Form:
TABLET
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
500 mg/1
-
Substance:
ACETAMINOPHEN
-
Start Marketing Date:
2025-11-06
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Shijiazhuang Lonzeal Pharmaceuticals Co., Ltd.
-
NDC:
55773-6031
-
Nonproprietary Name:
Paroxetine Hydrochloride Hemihydrate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
PAROXETINE HYDROCHLORIDE HEMIHYDRATE
-
Start Marketing Date:
2026-06-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
SHILPA PHARMA LIFESCIENCES LIMITED
-
NDC:
82920-717
-
Nonproprietary Name:
Ambroxol Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
AMBROXOL HYDROCHLORIDE
-
Start Marketing Date:
2026-05-10
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Create a New Buying Request
Fields marked with * are mandatory.