www.ndcvalidator.com
National Drug Code Lookup
|
NDC Directory
|
About
|
Feedback
"69953-516-01" National Drug Code (NDC)
Morning After 1 BLISTER PACK in 1 CARTON (69953-516-01) / 1 mg in 1 BLISTER PACK
(Rapha Pharmaceuticals, Inc.)
NDC Code
69953-516-01
Package Description
1 BLISTER PACK in 1 CARTON (69953-516-01) / 1 mg in 1 BLISTER PACK
Product NDC
69953-516
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Morning After
Non-Proprietary Name
Levonorgestrel
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20221230
Marketing Category Name
ANDA
Application Number
ANDA205329
Manufacturer
Rapha Pharmaceuticals, Inc.
Substance Name
LEVONORGESTREL
Strength
1.5
Strength Unit
mg/1.5mg
Pharmacy Classes
Inhibit Ovum Fertilization [PE], Progesterone Congeners [CS], Progesterone Congeners [CS], Progestin [EPC], Progestin-containing Intrauterine Device [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69953-516-01