Julie Morning After Pill
- Product NDC
- 82791-003
- 11-digit product format
- 827910003
- Labeler code
- 82791
- Product ID
- 82791-003_d5234e03-ab41-43ed-9ce7-bfcac34e0c0b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- levonorgestrel
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Julie Products Inc.
- Application
- ANDA206867
- Marketing category
- ANDA
- Marketing start
- 2025-11-20
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Julie Morning After Pill
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LEVONORGESTREL | 1.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5W7SIA7YZW |
| Rxcui | 483325, 2606549 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82791-003-01 | Julie Morning After Pill | 1 in 1 CARTON | TABLET | 1 | | 2 |
| 82791-003-01 | Julie Morning After Pill | 1 in 1 BLISTER PACK | TABLET | 1 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82791-003-01 | 82791000301 | 1 BLISTER PACK in 1 CARTON (82791-003-01) / 1 TABLET in 1 BLISTER PACK | 1 blister pack | 2025-11-20 | No | No | Current |