Package 0220-2329-41

Brand: gratiola officinalis

Generic: gratiola officinalis
NDC Package

Package Facts

Identity

Package NDC 0220-2329-41
Digits Only 0220232941
Product NDC 0220-2329
Description

30 [hp_C] in 1 TUBE (0220-2329-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand gratiola officinalis
Generic gratiola officinalis
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0d5748-6cee-0f47-e063-6294a90a154e", "openfda": {"unii": ["BDD9991A36"], "spl_set_id": ["7acfd065-58b6-21f8-e053-2991aa0a252a"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-2329-41)", "package_ndc": "0220-2329-41", "marketing_start_date": "19830303"}], "brand_name": "Gratiola officinalis", "product_id": "0220-2329_0a0d5748-6cee-0f47-e063-6294a90a154e", "dosage_form": "PELLET", "product_ndc": "0220-2329", "generic_name": "GRATIOLA OFFICINALIS", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Gratiola officinalis", "active_ingredients": [{"name": "GRATIOLA OFFICINALIS", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}