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Ella
Ella - 52544-238-54 - (ulipristal acetate)
Drug Information of Ella
| Product NDC: | 52544-238 |
| Proprietary Name: | Ella |
| Non Proprietary Name: | ulipristal acetate |
| Active Ingredient(s): | 30 mg/1 & nbsp; ulipristal acetate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ella
| Product NDC: | 52544-238 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022474 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100813 |
Package Information of Ella
| Package NDC: | 52544-238-54 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (52544-238-54) > 1 TABLET in 1 BLISTER PACK |
NDC Information of Ella
| NDC Code | 52544-238-54 |
| Proprietary Name | Ella |
| Package Description | 1 BLISTER PACK in 1 CARTON (52544-238-54) > 1 TABLET in 1 BLISTER PACK |
| Product NDC | 52544-238 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ulipristal acetate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100813 |
| Marketing Category Name | NDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | ULIPRISTAL ACETATE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
