Product list field descriptions
Field name | Description | Sample |
---|---|---|
product_id | Medicine product ID | 00-0001-04 |
original_name | Original name of the medicine | Druniler 120 mg film-coated tablets |
medicine_name | Name of the medicine in Latvian | Druniler 120 mg apvalkotās tabletes |
short_name | Short name of the medicine | Druniler |
authorisation_no | Authorisation number | 00-0001 |
date_of_authorisation | Date of medicine authorisation, DD-MMM-YY | 26-APR-24 |
authorisation_validity_ttl | Authorisation validity date, DD-MMM-YY or „Uz neierobežotu laiku” (unlimited) | 26-APR-24 |
inter_code | Procedure number | EMEA/H/C/000471 |
legal_status | Oridination | Pr. |
legal_bases_code | Legal base (code) | 8 (3) p. |
legal_bases_text | Legal base in Latvian (text) | Pilns iesniegums - zināmai aktīvai vielai |
strength | Strength | 0.5 mg |
strength_lv | Strength in Latvian | 0,5 mg |
pharmaceutical_form | Pharmaceutical form | Hard capsule |
pharmaceutical_form_lv | Pharmaceutical form in Latvian | Cietās kapsulas |
is_approved_for_kids | Medicine usage is approved for children 0 – no 1 – yes 2 – not defined |
1 |
active_substance | Active substance | Ketorolacum, Phenylephrinum |
marketing_authorisation_holder | Marketing authorisation holder, country | Otsuka Pharmaceutical Netherlands B.V., Nīderlande |
manufacturer* | Seria manufacturer, country | Krka Polska Sp. z o.o., Poland; KRKA, d.d., Novo mesto, Slovenia |
parallel_importer | Parallel importer | ELPIS SIA |
parallel_importer_lv | Parallel importer, country in Latvian | ELPIS SIA, Latvija |
parallel_importer_en | Parallel importer, country in English | ELPIS SIA, Latvia |
parallel_distributor | Parallel distributor | ELPIS SIA |
parallel_distributor_lv | Parallel distributor, country in Latvian | ELPIS SIA, Latvija |
parallel_distributor_en | Parallel distributor, country in English | ELPIS SIA, Latvia |
exp_country_lv | Exporter country in Latvian | Rumānija |
exp_country_en | Exporter country in English | Romania |
status | Status of the medicine 0 – authorisation withdrawn 1 – authorisation valid 2 – distributor of the medicine suspended |
1 |
remove_date | Date of authorisation withdrawal, YYYY.MM.DD | 2024.04.26 |
sell_stop_date | Distribution of medicine permitted until, YYYY.MM.DD | 2024.04.26 |
prd_removed | Status of medicine product 0 – on the registry 1 – withdrawn from the registry |
0 |
prd_sell_stop_date | Distribution of medicinal product permitted until, YYYY.MM.DD | 2024.04.26 |
atc_code* | ATC code | C10AB05 |
authorisation_procedure | Authorisation procedure | Eiropas centralizētā reģistrācijas procedūra |
package_leaflet | Link to the current package leaflet (PDF, Word or other format) | https://dati.zva.gov.lv/zalu-registrs/info/00-0001/pil |
summary_of_product_characteristics | Link to the current summary of product characteristics leaflet (PDF, Word or other format) | https://dati.zva.gov.lv/zalu-registrs/info/00-0001/smpc |
product_strength | Product strength | 300 mg |
store_conditions* | Storing conditions | Uzglabāt temperatūrā līdz 30 °C.; Uzglabāt oriģinālā iepakojumā. |
package | Primary packaging | Kartona kastīte, Alumīnija tūba, N10 |
package_en | Primary packaging in English | Carton box, Aluminium tube, N10 |
package_size | Package size | 20 |
labels* | Link to the document containing texts for the label | |
package_labels* | Link to the package labels | |
container_labels* | Link to the container labels | |
product_price_without_vat_eur | Maximum admissible pharmacy price (€ excl. VAT) | 12.33 |
product_price_with_vat_eur | Maximum admissible pharmacy price (€ incl. VAT) | 12.33 |
* If the field contains more than one value, they are split by semicolon.