Package 0220-3900-41

Brand: paeonia officinalis

Generic: paeonia officinalis root
NDC Package

Package Facts

Identity

Package NDC 0220-3900-41
Digits Only 0220390041
Product NDC 0220-3900
Description

6 [hp_C] in 1 TUBE (0220-3900-41)

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0b34ba-2f56-27a4-e063-6394a90a0777", "openfda": {"unii": ["8R564U2E1P"], "spl_set_id": ["7f72441a-dfb4-1e5a-e053-2a91aa0a39db"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (0220-3900-41)", "package_ndc": "0220-3900-41", "marketing_start_date": "19830303"}], "brand_name": "Paeonia officinalis", "product_id": "0220-3900_0a0b34ba-2f56-27a4-e063-6394a90a0777", "dosage_form": "PELLET", "product_ndc": "0220-3900", "generic_name": "PAEONIA OFFICINALIS ROOT", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Paeonia officinalis", "active_ingredients": [{"name": "PAEONIA OFFICINALIS ROOT", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}