Menopause

Product NDC
54973-9113
11-digit product format
549739113
Labeler code
54973
Product ID
54973-9113_602dd304-758b-3875-e053-2991aa0ab369
Type
HUMAN OTC DRUG
Nonproprietary name
amyl nitrite, sanguinaria canadensis root, and lachesis muta venom
Dosage form
TABLET, SOLUBLE
Route
ORAL
Labeler
Hyland's
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-03-01
Marketing end
0000-00-00
Substance
AMYL NITRITE; SANGUINARIA CANADENSIS ROOT; LACHESIS MUTA VENOM
Active strength
6 [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC exclude flag
No
Listing certified through
2020-12-31
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.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct54973-9113DDiscontinued by firm2026-07-31
excluded packagepackage54973-911354973-9113-2DDiscontinued by firm2026-07-31

DailyMed Socrata Ingredients#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
54973-9113-254973911302100 TABLET, SOLUBLE in 1 BOTTLE, PLASTIC (54973-9113-2) 1995-03-010000-00-00NoNoCurrent