Miers Laboratories
NDC Database

Miers Laboratories

NDC Database

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

Drug for Further Processing
  • Total Records 5
  • Latest Marketing Date 2022-12-02
  • Data Source FDA
  • First Marketing Date 2019-03-04
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Company

Miers Laboratories

Country

New Zealand

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Company Snapshot

Miers Laboratories

Wellington

New Zealand

www.mierslabs.co.nz/ View on Map
NDC Records ( 5 records )
2022
02 Dec
Drug for Further Processing NDC: 59672-0016

Nonproprietary Name

arnica montana whole, rhododendron tomentosum leafy twig, toxicodendron pubescens leaf, and ruta graveolens flowering top

Dosage Form

TABLET

Strength

30; 30; 30; 30 1; 1; 1; 1

Labeler

Miers Laboratories

Marketing Category

DRUG FOR FURTHER PROCESSING

59672-0016

Substance

ARNICA MONTANA WHOLE; RHODODENDRON TOMENTOSUM LEAFY TWIG; RUTA GRAVEOLENS FLOWERING TOP; TOXICODENDRON PUBESCENS LEAF

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2022-12-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
04 Mar
Drug for Further Processing NDC: 59672-1116

Nonproprietary Name

Arnica Montana, Bellis Perennis, Matricaria Chamomilla, Ipecac, and Lycopdoium clavatum spore

Dosage Form

TABLET

Strength

30; 30; 30; 30; 30 1; 1; 1; 1; 1

Labeler

Miers Laboratories

Marketing Category

DRUG FOR FURTHER PROCESSING

59672-1116

Substance

ARNICA MONTANA WHOLE; BELLIS PERENNIS WHOLE; IPECAC; LYCOPODIUM CLAVATUM SPORE; MATRICARIA CHAMOMILLA WHOLE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2019-03-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
01 May
Drug for Further Processing NDC: 59672-1316

Nonproprietary Name

arabica coffee bean, passiflora incarnata flowering top, and valerian

Dosage Form

TABLET

Strength

6; 6; 250 1; 1; mg/1

Labeler

Miers Laboratories

Marketing Category

DRUG FOR FURTHER PROCESSING

59672-1316

Substance

ARABICA COFFEE BEAN; PASSIFLORA INCARNATA FLOWERING TOP; VALERIAN

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2021-05-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
06 Dec
Drug for Further Processing NDC: 59672-1716

Nonproprietary Name

sodium borate, anamirta cocculus seed, gelsemium sempervirens root, wood creosote, toxicodendron pubescens leaf, and tobacco leaf

Dosage Form

TABLET

Strength

30; 30; 30; 30; 30; 30 1; 1; 1; 1; 1; 1

Labeler

Miers Laboratories

Marketing Category

DRUG FOR FURTHER PROCESSING

59672-1716

Substance

ANAMIRTA COCCULUS SEED; GELSEMIUM SEMPERVIRENS ROOT; SODIUM BORATE; TOBACCO LEAF; TOXICODENDRON PUBESCENS LEAF; WOOD CREOSOTE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2019-12-06

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
02 Dec
Drug for Further Processing NDC: 59672-2516

Nonproprietary Name

ACTIVATED CHARCOAL, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, and STRYCHNOS NUX-VOMICA SEED

Dosage Form

TABLET

Strength

30; 30; 30 1; 1; 1

Labeler

Miers Laboratories

Marketing Category

DRUG FOR FURTHER PROCESSING

59672-2516

Substance

ACTIVATED CHARCOAL; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; STRYCHNOS NUX-VOMICA SEED

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2022-12-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
5 total
  • Drug for Further Processing
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

59672-0016

Nonproprietary Name

arnica montana whole, rhododendron tomentosum leafy twig, toxicodendron pubescens leaf, and ruta graveolens flowering top

Labeler

Miers Laboratories

Dosage Form

TABLET

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

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