Fallback Solo

Product NDC
68180-853
11-digit product format
681800853
Labeler code
68180
Product ID
68180-853_90e6df86-1943-416d-835e-868385efeb15
Type
HUMAN OTC DRUG
Nonproprietary name
levonorgestrel
Dosage form
TABLET
Route
ORAL
Labeler
Lupin Pharmaceuticals, Inc.
Application
ANDA201446
Marketing category
ANDA
Marketing start
2014-07-22
Marketing end
0000-00-00
Substance
LEVONORGESTREL
Active strength
2 mg/1
Pharmacologic classes
Inhibit Ovum Fertilization [PE], Progesterone Congeners [CS], Progesterone Congeners [CS], Progestin [EPC], Progestin-containing Intrauterine Device [EPC]
NDC exclude flag
No
Listing certified through
2024-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68180-853-11EA - Each68180-853a7e71e8c-c6de-4a8c-8c63-32f0a4264d5812014-10-03
68180-853-13EA - Each68180-85398033c05-e1c1-48a6-8eea-4c2b868e5a7a12014-10-03

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68180-853-13681800853131 BLISTER PACK in 1 CARTON (68180-853-13) > 1 TABLET in 1 BLISTER PACK (68180-853-11) 1 blister pack2014-07-220000-00-00NoNoCurrent