EDP INDIGO

Product NDC
70434-102
11-digit product format
704340102
Labeler code
70434
Product ID
70434-102_7f899eae-76f5-a1e8-e053-2991aa0a0c09
Type
HUMAN OTC DRUG
Nonproprietary name
Indigofera Tinctoria Leaf
Dosage form
POWDER
Route
TOPICAL
Labeler
EDP Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2016-02-01
Marketing end
0000-00-00
Substance
INDIGOFERA TINCTORIA LEAF
Active strength
1 1/100g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70434-102-022021-01-29C16284748780-1ba0f9c33-2452-a910-e053-dadaa90a0b85EDP INDIGO

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70434-102-01EDP INDIGO100 g in 1 BAGPOWDER1004
70434-102-02EDP INDIGO1 in 1 PACKAGEPOWDER14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70434-102EDP INDIGO (INDIGOFERA TINCTORIA LEAF) POWDER [EDP INC.]4Legacy NDC, 2 package rows20190116_036fa661-b076-41c6-a303-b4cd1de634f3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
70434-102-0170434010201100 g in 1 BAG100 gHistorical
70434-102-02704340102021 in 1 PACKAGEHistorical