MINIVLAR 30
- Product NDC
- 72689-0011
- 11-digit product format
- 726890011
- Labeler code
- 72689
- Product ID
- 72689-0011_7b38aa8b-0c8a-66b1-e053-2991aa0aeac8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethinyl Estradiol, Levonorgestrel
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- OASIS TRADING
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2018-11-21
- Marketing end
- 0000-00-00
- Substance
- ETHINYL ESTRADIOL; LEVONORGESTREL
- Active strength
- 0 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 72689-0011-1 | MINIVLAR 30 | 21 in 1 BLISTER PACK | TABLET | 21 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72689-0011 | MINIVLAR 30 (ETHINYL ESTRADIOL, LEVONORGESTREL) TABLET [OASIS TRADING] | 1 | Legacy NDC, 1 package rows | 20181122_f4264944-56c5-4f95-a8d7-8ded02953043.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 72689-0011-1 | 72689001101 | 21 in 1 BLISTER PACK | Historical |