After Banger
- Product NDC
- 58602-891
- 11-digit product format
- 586020891
- Labeler code
- 58602
- Product ID
- 58602-891_3943f64a-38c2-43c7-8593-9f850051a98a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Levonorgestrel
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aurohealth LLC
- Application
- ANDA206867
- Marketing category
- ANDA
- Marketing start
- 2023-03-23
- 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 System [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 |
|---|
| 58602-891-57 | 58602089157 | 1 BLISTER PACK in 1 CARTON (58602-891-57) / 1 TABLET in 1 BLISTER PACK | 1 blister pack | 2023-03-23 | No | No | Historical |
| 58602-891-69 | 58602089169 | 1 BLISTER PACK in 1 CARTON (58602-891-69) / 1 TABLET in 1 BLISTER PACK | 1 blister pack | 2023-03-23 | No | No | Historical |