AfterPlan
- Product NDC
- 62756-723
- 11-digit product format
- 627560723
- Labeler code
- 62756
- Product ID
- 62756-723_f86715c5-932d-405d-b81d-286c86409b1e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- levonorgestrel
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- SUN PHARMACEUTICAL INDUSTRIES, INC.
- Application
- ANDA202635
- Marketing category
- ANDA
- Marketing start
- 2017-05-12
- Substance
- LEVONORGESTREL
- Active strength
- 1.5 mg/1
- Pharmacologic classes
- Inhibit Ovum Fertilization [PE], Progesterone Congeners [CS], Progesterone Congeners [CS], Progestin [EPC], Progestin-containing Intrauterine Device [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 5W7SIA7YZW | LEVONORGESTREL | 797-63-7 | LEVONORGESTREL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 62756-723-60 | 62756072360 | 1 BLISTER PACK in 1 CARTON (62756-723-60) / 1 TABLET in 1 BLISTER PACK | 1 blister pack | 2017-05-12 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| AfterPlan™ | SUN PHARMACEUTICAL INDUSTRIES, INC. | Sun Pharmaceutical Industries Limited | 2018-10-26 | HUMAN OTC DRUG LABEL | 2 |