Home NDC 48951-3020-3 Carbo Betulae 20 Special Order
Product NDC 48951-3020
Requested package NDC 48951-3020-3
11-digit product format 489513020
Labeler code 48951
Product ID 48951-3020_6a89a525-6c9d-4ad2-e053-2a91aa0afeb9
Type HUMAN OTC DRUG
Nonproprietary name Carbo Betulae 20 Special Order
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Marketing end 0000-00-00
Substance ACTIVATED CHARCOAL
Active strength 20 [hp_X]/mL
NDC exclude flag No
Listing certified through 2020-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 48951-3020 48951-3020-3 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 48951-3020 48951-3020-3 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-3020 CARBO BETULAE 20 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.] 2 Legacy NDC 20180424_834847f1-cca2-477e-85be-b0b2ebf0731e.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 48951-3020-3 48951302003 60 mL in 1 BOTTLE, DROPPER (48951-3020-3) 60 ml 2009-09-01 0000-00-00 No No Current