aconitum e tub. 30

Generic: aconitum e tub. 30

Labeler: uriel pharmacy inc.
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name aconitum e tub. 30
Generic Name aconitum e tub. 30
Labeler uriel pharmacy inc.
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

aconitum napellus 30 [hp_X]/mL

Manufacturer
Uriel Pharmacy Inc.

Identifiers & Regulatory

Product NDC 48951-1338
Product ID 48951-1338_42f33cb7-d6d8-783a-e063-6294a90a3794
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 2009-09-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 489511338
Hyphenated Format 48951-1338

Supplemental Identifiers

UNII
U0NQ8555JD

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name aconitum e tub. 30 (source: ndc)
Generic Name aconitum e tub. 30 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 [hp_X]/mL
source: ndc
Packaging
  • 10 AMPULE in 1 BOX (48951-1338-1) / 1 mL in 1 AMPULE
source: ndc

Packages (1)

48951-1338-1 10 AMPULE in 1 BOX (48951-1338-1) / 1 mL in 1 AMPULE

Ingredients (1)

aconitum napellus (30 [hp_X]/mL)

Linked Drug Pages (1)

Aconitum e tub. 30 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "42f33cb7-d6d8-783a-e063-6294a90a3794", "openfda": {"unii": ["U0NQ8555JD"], "spl_set_id": ["8b80552a-6ae3-40ea-bf41-5cd705be04f2"], "manufacturer_name": ["Uriel Pharmacy Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 BOX (48951-1338-1)  / 1 mL in 1 AMPULE", "package_ndc": "48951-1338-1", "marketing_start_date": "20090901"}], "brand_name": "Aconitum e tub. 30", "product_id": "48951-1338_42f33cb7-d6d8-783a-e063-6294a90a3794", "dosage_form": "LIQUID", "product_ndc": "48951-1338", "generic_name": "Aconitum e tub. 30", "labeler_name": "Uriel Pharmacy Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aconitum e tub. 30", "active_ingredients": [{"name": "ACONITUM NAPELLUS", "strength": "30 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}