Product NDC: | 51285-204 |
Proprietary Name: | ParaGard T 380A |
Non Proprietary Name: | copper |
Active Ingredient(s): | 313.4 mg/1 & nbsp; copper |
Administration Route(s): | INTRAUTERINE |
Dosage Form(s): | INTRAUTERINE DEVICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51285-204 |
Labeler Name: | Teva Women's Health, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018680 |
Marketing Category: | NDA |
Start Marketing Date: | 19841101 |
Package NDC: | 51285-204-01 |
Package Description: | 1 INTRAUTERINE DEVICE in 1 CARTON (51285-204-01) |
NDC Code | 51285-204-01 |
Proprietary Name | ParaGard T 380A |
Package Description | 1 INTRAUTERINE DEVICE in 1 CARTON (51285-204-01) |
Product NDC | 51285-204 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | copper |
Dosage Form Name | INTRAUTERINE DEVICE |
Route Name | INTRAUTERINE |
Start Marketing Date | 19841101 |
Marketing Category Name | NDA |
Labeler Name | Teva Women's Health, Inc. |
Substance Name | COPPER |
Strength Number | 313.4 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Copper [Chemical/Ingredient],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE] |