FDA.reportPublic FDA data

HanPoong Beat Cold

Product NDC
82369-1111
11-digit product format
823691111
Labeler code
82369
Product ID
82369-1111_d07b3324-c87d-bb7a-e053-2a95a90a3d51
Type
HUMAN OTC DRUG
Nonproprietary name
Ephedrine HCI
Dosage form
TABLET
Route
ORAL
Labeler
HANPOONG PHARM CO.,LTD.
Application
part349
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2022-01-01
Marketing end
0000-00-00
Substance
EPHEDRINE HYDROCHLORIDE
Active strength
5 mg/8g
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct82369-1111DDiscontinued by firm2026-08-03
excluded packagepackage82369-111182369-1111-1DDiscontinued by firm2026-08-03

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
82369-1111-1823691111011 POUCH in 1 BOX (82369-1111-1) > 16 g in 1 POUCH (82369-1111-2) 1 pouch2022-01-010000-00-00NoNoCurrent