MaxFe

Product NDC
67555-140
11-digit product format
675550140
Labeler code
67555
Product ID
67555-140_a769b672-5a74-4d2a-a01a-e7c3c124d94e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ascorbic acid, folic acid, vitamin b-12, biotin, iron, magnesium, zinc
Dosage form
TABLET
Route
ORAL
Labeler
Pronova Corporation
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2014-06-01
Marketing end
0000-00-00
Substance
ASCORBIC ACID; FOLIC ACID; CYANOCOBALAMIN; BIOTIN; IRON; MAGNESIUM; ZINC; DOCUSATE SODIUM
Active strength
100 mg/1; mg/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1
Pharmacologic classes
Vitamin C [EPC],Ascorbic Acid [CS],Vitamin B 12 [CS],Vitamin B12 [EPC]
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
67555-140-122020-02-18C16284748780-19d75b9d1-2271-f424-e053-dadaa90a57ce0883e94f-7987-4a17-a7c1-70655d827c17
67555-140-122020-01-31C16284748780-19d75b9d1-2271-f424-e053-dadaa90a57ce0883e94f-7987-4a17-a7c1-70655d827c17

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
67555-140-12EA - Each67555-140cada1f35-bc78-4284-836c-c00a354e673a12014-07-02