2.9.5. UNIFORMITY OF MASS OF SINGLE-DOSE PREPARATIONS

5.1.4. MICROBIOLOGICAL QUALITY OF …

5.1.4. Microbiological quality of pharmaceutical preparations EUROPEAN PHARMACOPOEIA 6.0 B. Herbal medicinal products to which boiling water is not added before use. — Total viable aerobic count (2.6.12).Not more than 105 bacteria and not more than 104 fungi per gram or per millilitre. —Notmorethan103 enterobacteria …

  Pharmaceutical, Preparation, Medicinal, Herbal, Herbal medicinal, Pharmaceutical preparations

2.2.24. Absorption spectrophotometry, infrared - …

2.2.24. Absorption spectrophotometry, infrared EUROPEAN PHARMACOPOEIA 6.0 PREPARATION OF THE SAMPLE FOR RECORDING BY TRANSMISSION OR ABSORPTION Prepare the substance by one of the following methods.

  Infrared, Absorption, Absorption spectrophotometry, Spectrophotometry

2.2.25. ABSORPTION SPECTROPHOTOMETRY, …

2.2.25. Absorption spectrophotometry, ultraviolet and visible EUROPEAN PHARMACOPOEIA 6.0 permitted tolerance is ± 1 nm for the ultraviolet range and ± 3 nm for the visible range.

  Ultraviolet, Absorption, Visible, Absorption spectrophotometry, Spectrophotometry, Ultraviolet and visible

2.9.36. POWDER FLOW - uspbpep.com

2.9.36. Powder flow EUROPEAN PHARMACOPOEIA 6.0 since the lattice parameters are comparatively large, the symmetry is low and the scattering properties are …

EUROPEAN PHARMACOPOEIA 5 - uspbpep.com

EUROPEAN PHARMACOPOEIA 5.0 2.9.2. Disintegration of suppositories and pessaries to a mechanical device capable of raising and lowering it smoothly at constant frequency between 29 and 32 cycles

  European, Pharmacopoeia, Suppositories, European pharmacopoeia

LACTOSE MONOHYDRATE - uspbpep.com

EUROPEAN PHARMACOPOEIA 5.0 Lactose monohydrate Bulkandtappeddensity(2.9.15).Determine the bulk density and the tapped density. Calculate the Hausner index using the following expression:

  Lactose monohydrate, Lactose, Monohydrate, Uspbpep

2.2. PHYSICAL AND PHYSICOCHEMICAL METHODS

2.2.2. Degree of coloration of liquids EUROPEAN PHARMACOPOEIA 6.0 made lie in the range of 1750-2000 NTU. Linearity must be demonstrated by constructing a calibration curve using at

  Using, Methods, Physical, Physicochemical, Physical and physicochemical methods

MAIZE STARCH - uspbpep.com

Maize oil, refined EUROPEAN PHARMACOPOEIA 6.0 Chlorides (2.4.4): maximum 500 ppm. Dilute 0.5 ml of solution S to 15 ml withwater R.Prepare the standard using a mixture of 5 ml ofchloride standard

  Starch

Conductivity Aqua purificata (°C) (µS·cm 1

EUROPEAN PHARMACOPOEIA 5.0 Water, purified Heavy metals(2.4.8): maximum 0.1 ppm. Heat 200 ml in a glass evaporating dish on a water-bath until the volume is reduced to 20 ml. 12 ml of the concentrated

  Water, Aqua, Conductivity, Purified, Conductivity aqua purificata, Purificata

2.2.32. LOSS ON DRYING - uspbpep.com

EUROPEAN PHARMACOPOEIA 6.0 2.2.32. Loss on drying using the conditions recommended by the manufacturer of the equipment. Manufacturers of SDS …

  Drying

2.9.40. UNIFORMITY OF DOSAGE UNITS - uspbpep.com

2.9.40. UNIFORMITY OF DOSAGE UNITS To ensure the consistency of dosage units, each unit in a batch should have an active substance content within a narrow range around the label claim. Dosage units are defined as dosage forms containing a single dose or a part of a dose of an active substance in each dosage unit. The

  Unit, Dosage, Uniformity, Uniformity of dosage units, Dosage units, Of dosage units