Home NDC 83641-001 Anatra
Product NDC 83641-001
11-digit product format 836410001
Labeler code 83641
Product ID 83641-001_4097d2e5-5d3f-b62a-e063-6294a90a882f
Type HUMAN OTC DRUG
Nonproprietary name Anas Barbariae
Dosage form TABLET
Route ORAL
Labeler Anatra LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2023-09-01
Substance CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE
Active strength 200 [hp_C]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 · 3 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 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 83641-001 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 83641-001 83641-001-01 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 83641-001 83641-001-02 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base Anatra
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE 200 [hp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination RN2HC612GY Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83641-001-01 Anatra 30 in 1 BOTTLE, PLASTIC TABLET 30 3 83641-001-02 Anatra 60 in 1 BOTTLE, PLASTIC TABLET 60 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83641-001 ANATRA (ANAS BARBARIAE) TABLET [ANATRA LLC] 2 Current NDC, 2 package rows 20250115_4562fa87-ed88-42fb-b530-e600aea351d9.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 83641-001-01 83641000101 30 TABLET in 1 BOTTLE, PLASTIC (83641-001-01) 30 tablet 2023-09-01 No No Current 83641-001-02 83641000102 60 TABLET in 1 BOTTLE, PLASTIC (83641-001-02) 60 tablet 2023-09-01 No No Current