PostDay One-Step
- Product NDC
- 69953-616
- 11-digit product format
- 699530616
- Labeler code
- 69953
- Product ID
- 69953-616_6f7f3ed2-ae0b-88ca-e053-2a91aa0a8b7d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Levonorgestrel
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rapha Pharmaceuticals, Inc.
- Application
- ANDA206867
- Marketing category
- ANDA
- Marketing start
- 2018-07-01
- Marketing end
- 0000-00-00
- Substance
- LEVONORGESTREL
- Active strength
- 2 mg/1.5mg
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69953-616-01 | 69953061601 | 1 BLISTER PACK in 1 CARTON (69953-616-01) > 1 mg in 1 BLISTER PACK | 1 blister pack | 2018-07-01 | 0000-00-00 | No | No | Current |