| 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] |