Aftera 1.5 mg/1
LEVONORGESTREL · TABLET · Foundation Consumer Healthcare LLC
No Recall History
Plain English
Aftera is a tablet containing levonorgestrel at 1.5 mg/1, taken oral. Manufactured by Foundation Consumer Healthcare LLC.
Key Facts
- Brand Name
- Aftera
- Generic Name
- LEVONORGESTREL
- NDC Code (Product)
69536-103- Manufacturer
- Foundation Consumer Healthcare LLC
- Strength
- 1.5 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- NDA021998
- Drug Class
- Progestin [EPC]; Progestin-containing Intrauterine System [EPC]
- Marketing Start
- 05/10/2018
Recall History
No Recall HistoryFrequently Asked Questions
What is Aftera used for?
Aftera contains LEVONORGESTREL. It is a tablet taken oral. Consult your doctor for specific uses.
Is Aftera a controlled substance?
Aftera is not classified as a controlled substance by the DEA.
What is the generic name for Aftera?
The generic name for Aftera is LEVONORGESTREL. There are 12 other brand versions of LEVONORGESTREL.
What is the NDC code for Aftera 1.5 mg/1?
The NDC (National Drug Code) for Aftera 1.5 mg/1 is 69536-103, listed by Foundation Consumer Healthcare LLC.
Other Levonorgestrel Brands
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- camrese Lo0093-6148
- levonorgestrel and ethinyl estradiol42192-623
- My Way1.5 mg/143386-622
- Kurvelo50090-6374
- Econ Morning After1.5 mg/158602-841
- My Choice TM1.5 mg/162756-720
- Kurvelo68180-844
- LEVONORGESTREL AND ETHINYL ESTRADIOL AND ETHINYL ESTRADIOL0378-7284
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)