Zhejiang Huahai Pharmaceutical
NDC Database

Zhejiang Huahai Pharmaceutical

NDC Database

National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.

Bulk Ingredient
  • Total Records 3
  • Latest Marketing Date 2021-04-01
  • Data Source FDA
  • First Marketing Date 2014-04-16
Company Overview

Company

Zhejiang Huahai Pharmaceutical

Country

China

Social Profiles

Company Snapshot

Zhejiang Huahai Pharmaceutical

Xunqiao, Linhai, Zhejiang 317024

China

en.huahaipharm.com:443/ sales@huahaipharm.com View on Map
NDC Records ( 3 records )
2021
01 Apr
Bulk Ingredient NDC: 64220-993

Nonproprietary Name

Ropinirole 5% w/w Triturate with Lactose

Dosage Form

POWDER

Strength

0.0057 kg/.1kg

Labeler

Zhejiang Huahai Pharmaceutical Co., LTD

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

64220-993

Substance

ROPINIROLE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-04-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
16 Apr
Bulk Ingredient NDC: 64220-995

Nonproprietary Name

rizatriptan benzoate

Dosage Form

TABLET

Strength

10 mg/1

Labeler

Zhejiang Huahai Pharmaceutical Co., LTD

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

64220-995

Substance

RIZATRIPTAN BENZOATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-04-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
16 Apr
Bulk Ingredient NDC: 64220-996

Nonproprietary Name

rizatriptan benzoate

Dosage Form

TABLET

Strength

5 mg/1

Labeler

Zhejiang Huahai Pharmaceutical Co., LTD

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

64220-996

Substance

RIZATRIPTAN BENZOATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-04-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
3 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 Record Details Preview

Explore important National Drug Code information available in the records above.

NDC

64220-993

Nonproprietary Name

Ropinirole 5% w/w Triturate with Lactose

Labeler

Zhejiang Huahai Pharmaceutical Co., LTD

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

Regular Updates

Data maintained from official sources

Structured Database

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Reliable Data

Organized NDC records

NDC data is based on publicly available U.S. Food and Drug Administration (FDA) National Drug Code information.

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