Take Action
- Product NDC
- 69536-200
- 11-digit product format
- 695360200
- Labeler code
- 69536
- Product ID
- 69536-200_2e871e24-100b-4a74-959d-8df23d97e979
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- levonorgestrel
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Foundation Consumer Healthcare LLC
- Application
- NDA021998
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2018-05-10
- 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 |
|---|
| 69536-200-88 | 69536020088 | 1 BLISTER PACK in 1 BOX, UNIT-DOSE (69536-200-88) / 1 TABLET in 1 BLISTER PACK | 1 blister pack | 2018-05-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Take Action ® | Foundation Consumer Healthcare LLC | 2023-01-31 | HUMAN OTC DRUG LABEL | 5 |