69536-103 : Aftera 1.5 mg Oral Tablet
NDC: | 69536-103 |
Labeler: | Foundation Consumer Healthcare LLC |
Product Type: | Human OTC Drug |
Drug Name: | Aftera |
Dosage Form: | Oral Tablet |
Application #: | NDA021998 |
Rev. Date: |
Appearance:
Markings: | G00 |
Shapes: |
Round |
Colors: |
White |
Size (mm): | 8 |
Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 69536-103-88: 1 BLISTER PACK IN 1 BOX, UNIT‑DOSE (69536‑103‑88) > 1 TABLET IN 1 BLISTER PACK
Active Ingredients:
- Levonorgestrel
Dosage Strength:
- 1.5 mg
Inactive Ingredients:
- Silicon Dioxide
- Starch, Potato
- Magnesium Stearate
- Talc
- Starch, Corn
- Lactose Monohydrate /
Pharmaceutical Classes:
- Inhibit Ovum Fertilization [PE]
- Progesterone Congeners [CS]
- Progestin [EPC]
- Progestin-containing Intrauterine Device [EPC]
Related Products:
Based on records with the same trade name.- 51285-103 Aftera 1.5 mg Oral Tablet by Teva Women's Health, Inc.
NDC QR Code
Scan the QR code below to easily reference this data in the future:< Prev: 69536-100Next: 69536-108 >
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.