Ammonia Inhalant

Product NDC
55670-710
11-digit product format
556700710
Labeler code
55670
Product ID
55670-710_cc6eb737-6715-7cd2-e053-2995a90af54c
Type
HUMAN OTC DRUG
Nonproprietary name
Ammonia
Dosage form
AEROSOL
Route
RESPIRATORY (INHALATION)
Labeler
Moore Medical LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2017-11-29
Marketing end
2025-01-01
Substance
AMMONIA
Active strength
0 g/.3mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55670-710-012020-03-28C16284748780-19d75b9d0-c3f7-f424-e053-dadaa90a57ce5f261011-eec3-59fd-e053-2a91aa0a8e54
55670-710-012020-01-31C16284748780-19d75b9d0-c3f7-f424-e053-dadaa90a57ce5f261011-eec3-59fd-e053-2a91aa0a8e54

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55670-710-0155670071001100 CAPSULE in 1 BOX (55670-710-01) > .3 mL in 1 CAPSULE100 capsule2017-11-290000-00-00NoNoCurrent