Levonorgestrel
- Product NDC
- 49615-017
- 11-digit product format
- 496150017
- Labeler code
- 49615
- Product ID
- 49615-017_80b385e7-fe59-49b4-9de2-3c1ce3694cca
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Levonorgestrel
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- OC Pharma, LLC
- Application
- ANDA202380
- Marketing category
- ANDA
- Marketing start
- 2018-12-01
- Marketing end
- 0000-00-00
- Substance
- LEVONORGESTREL
- Active strength
- 2 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 49615-017-01 | Levonorgestrel | 1 in 1 CARTON | TABLET | 1 | | 1 |
| 49615-017-01 | Levonorgestrel | 1 in 1 BLISTER PACK | TABLET | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49615-017 | LEVONORGESTREL TABLET [OC PHARMA, LLC] | 1 | Legacy NDC, 2 package rows | 20181201_c7698816-6ac6-48c6-aaff-c484ebbafed3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 49615-017-01 | 49615001701 | 1 in 1 CARTON | Historical |