Morning After Pill 1.5 mg/1
levonorgestrel · TABLET · Cadence Health Inc
Morning After Pill is a tablet containing levonorgestrel at 1.5 mg/1, taken oral. Manufactured by Cadence Health Inc.
Key Facts
- Brand Name
- Morning After Pill
- Generic Name
- levonorgestrel
- NDC Code (Product)
73436-2859- Manufacturer
- Cadence Health Inc
- Strength
- 1.5 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- ANDA202380
- Drug Class
- Progestin [EPC]; Progestin-containing Intrauterine System [EPC]
- Marketing Start
- 10/01/2023
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Full Prescribing Information
Indications & Usage
Use for women to reduce chance of pregnancy after unprotected sex (if a contraceptive failed or if you did not use birth control)
Dosage & Administration
Directions take as soon as possible within 72 hours (3 days) after unprotected sex. The sooner you take it, the better it will work. if you vomit within 2 hours of taking the medication, call a healthcare professional to find out if you should repeat that dose
Warnings
Warnings Allergy Alert: Do not use if you have ever had an allergic reaction to levonorgestrel Sexually transmitted diseases (STDs) Alert: This product does not protect against HIV/AIDS or other STDs
Frequently Asked Questions
What is Morning After Pill used for?
Morning After Pill contains levonorgestrel. It is a tablet taken oral. Consult your doctor for specific uses.
Is Morning After Pill a controlled substance?
Morning After Pill is not classified as a controlled substance by the DEA.
What is the generic name for Morning After Pill?
The generic name for Morning After Pill is levonorgestrel. There are 11 other brand versions of levonorgestrel.
What is the NDC code for Morning After Pill 1.5 mg/1?
The NDC (National Drug Code) for Morning After Pill 1.5 mg/1 is 73436-2859, listed by Cadence Health Inc.