ASCORBIC ACID

Product NDC
71414-115
11-digit product format
714140115
Labeler code
71414
Product ID
71414-115_531e585f-55e3-6f37-e054-00144ff88e88
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ASCORBIC ACID
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Labeler
FLON LABORATORIES LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2017-04-01
Marketing end
0000-00-00
Substance
ASCORBIC ACID
Active strength
500 mg/mL
Pharmacologic classes
Vitamin C [EPC],Ascorbic Acid [CS]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71414-115-012024-12-12C16284748780-19d75b9d1-0f75-f424-e053-dadaa90a57ce4eb6a932-244e-30c5-e054-00144ff8d46c
71414-115-012020-01-31C16284748780-19d75b9d1-0f75-f424-e053-dadaa90a57ce4eb6a932-244e-30c5-e054-00144ff8d46c

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71414-115-01ML - Milliliter71414-115581a4b1e-f662-4f11-853c-4a820583923f12018-03-08