Package 0220-2835-41

Brand: kali bichromicum

Generic: potassium dichromate
NDC Package

Package Facts

Identity

Package NDC 0220-2835-41
Digits Only 0220283541
Product NDC 0220-2835
Description

1 [hp_M] in 1 TUBE (0220-2835-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand kali bichromicum
Generic potassium dichromate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0dfe8a-78d5-8525-e063-6394a90aff46", "openfda": {"unii": ["T4423S18FM"], "spl_set_id": ["8605f7a1-daea-a7f0-e053-2a91aa0adcd7"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 [hp_M] in 1 TUBE (0220-2835-41)", "package_ndc": "0220-2835-41", "marketing_start_date": "19830303"}], "brand_name": "Kali bichromicum", "product_id": "0220-2835_0a0dfe8a-78d5-8525-e063-6394a90aff46", "dosage_form": "PELLET", "product_ndc": "0220-2835", "generic_name": "POTASSIUM DICHROMATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali bichromicum", "active_ingredients": [{"name": "POTASSIUM DICHROMATE", "strength": "1 [hp_M]/[hp_M]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}