Lidocaine and Prilocaine Cream

Product NDC
70512-030
11-digit product format
705120030
Labeler code
70512
Product ID
70512-030_b8e1f543-5d18-08a7-e053-2a95a90ac740
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lidocaine and Prilocaine Cream
Dosage form
CREAM
Route
TOPICAL
Labeler
SOLA Pharmaceuticals
Application
ANDA205887
Marketing category
ANDA
Marketing start
2019-02-04
Marketing end
0000-00-00
Substance
LIDOCAINE; PRILOCAINE
Active strength
25 mg/g; mg/g
Pharmacologic classes
Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE],Amide Local Anesthetic [EPC],Amides [CS],Local Anesthesia [PE]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70512-030-30GM - Gram70512-0308d081213-c995-4154-b094-2901a3a6788912019-03-12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70512-030-30705120030301 TUBE in 1 CARTON (70512-030-30) > 30 g in 1 TUBE1 tube2019-02-040000-00-00NoNoCurrent