Pulmo 8

Product NDC
48951-8083
11-digit product format
489518083
Labeler code
48951
Product ID
48951-8083_6d0c3e0f-c8cb-f2de-e053-2a91aa0a8b4d
Type
HUMAN OTC DRUG
Nonproprietary name
Pulmo 8
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
SUS SCROFA LUNG
Active strength
8 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8083-1Pulmo 810 in 1 BOXLIQUID104
48951-8083-1Pulmo 81 mL in 1 AMPULELIQUID14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SUS SCROFA LUNGACTIVE INGREDIENT7GL3G1COB3PULMO 8 LIQUID [URIEL PHARMACY INC.]1
SUS SCROFA LUNGACTIVE MOIETY7GL3G1COB3PULMO 8 LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XPULMO 8 LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RPULMO 8 LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8083PULMO 8 LIQUID [URIEL PHARMACY INC.]4Legacy NDC, 2 package rows20231222_54b3808d-3af5-41c7-a387-dfaee6979dab.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8083-14895180830110 AMPULE in 1 BOX (48951-8083-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent