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LO/OVRAL-28
LO/OVRAL-28 - 0008-2514-02 - (norgestrel and ethinyl estradiol)
Drug Information of LO/OVRAL-28
| Product NDC: | 0008-2514 |
| Proprietary Name: | LO/OVRAL-28 |
| Non Proprietary Name: | norgestrel and ethinyl estradiol |
| Active Ingredient(s): | & nbsp; norgestrel and ethinyl estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LO/OVRAL-28
| Product NDC: | 0008-2514 |
| Labeler Name: | Wyeth Pharmaceuticals Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017802 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19760301 |
Package Information of LO/OVRAL-28
| Package NDC: | 0008-2514-02 |
| Package Description: | 6 BLISTER PACK in 1 CARTON (0008-2514-02) > 1 KIT in 1 BLISTER PACK (0008-2514-01) |
NDC Information of LO/OVRAL-28
| NDC Code | 0008-2514-02 |
| Proprietary Name | LO/OVRAL-28 |
| Package Description | 6 BLISTER PACK in 1 CARTON (0008-2514-02) > 1 KIT in 1 BLISTER PACK (0008-2514-01) |
| Product NDC | 0008-2514 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | norgestrel and ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19760301 |
| Marketing Category Name | NDA |
| Labeler Name | Wyeth Pharmaceuticals Company |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
