Home NDC 16714-572 leuprolide acetate
Product NDC 16714-572
11-digit product format 167140572
Labeler code 16714
Product ID 16714-572_585b897e-a1ed-418c-8c4e-96a385b9d72b
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name leuprolide acetate
Dosage form KIT
Labeler NorthStar RxLLC
Application ANDA078885
Marketing category ANDA
Marketing start 2022-08-01
Marketing end 0000-00-00
Active strength 0
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 16714-572-01 16714057201 1 KIT in 1 CARTON (16714-572-01) * 1 VIAL, MULTI-DOSE in 1 CARTON (16714-540-01) > 2.8 mL in 1 VIAL, MULTI-DOSE * 28 PACKET in 1 CARTON > 1 mL in 1 PACKET 1 kit 2022-08-01 0000-00-00 No No Current