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CRYSELLE
CRYSELLE - 54868-4851-0 - (norgestrel and ethinyl estradiol)
Drug Information of CRYSELLE
| Product NDC: | 54868-4851 |
| Proprietary Name: | CRYSELLE |
| 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 CRYSELLE
| Product NDC: | 54868-4851 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075840 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20031016 |
Package Information of CRYSELLE
| Package NDC: | 54868-4851-0 |
| Package Description: | 1 BLISTER PACK in 1 POUCH (54868-4851-0) > 1 KIT in 1 BLISTER PACK |
NDC Information of CRYSELLE
| NDC Code | 54868-4851-0 |
| Proprietary Name | CRYSELLE |
| Package Description | 1 BLISTER PACK in 1 POUCH (54868-4851-0) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 54868-4851 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | norgestrel and ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20031016 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
