Ciprofloxacin

Product NDC
16571-135
11-digit product format
165710135
Labeler code
16571
Product ID
16571-135_45ff37cf-bb29-4e8b-99b4-881967ef61b3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ciprofloxacin
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC; TOPICAL
Labeler
Pack Pharmaceuticals, LLC
Application
ANDA077568
Marketing category
ANDA
Marketing start
2010-09-15
Marketing end
0000-00-00
Substance
CIPROFLOXACIN HYDROCHLORIDE
Active strength
3 mg/mL
Pharmacologic classes
Quinolone Antimicrobial [EPC],Quinolones [CS]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
16571-135-10ML - Milliliter16571-135bc3e8b3c-641c-4f29-bfa2-a26812eb381b12012-07-24
16571-135-50ML - Milliliter16571-135226cd099-9d16-4db0-8ad3-bee819b5f5c512012-07-24