Progesterone
- Product NDC
- 69543-375
- 11-digit product format
- 695430375
- Labeler code
- 69543
- Product ID
- 69543-375_2ed02d5f-7930-444e-842f-207821d6b3e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Progesterone
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Virtus Pharmaceuticals
- Application
- NDA019781
- Marketing category
- NDA
- Marketing start
- 2016-07-13
- Marketing end
- 0000-00-00
- Substance
- PROGESTERONE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Progesterone [CS],Progesterone [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69543-375 | PROGESTERONE CAPSULE [VIRTUS PHARMACEUTICALS] | 6 | Legacy NDC | 20241120_2fac2189-5d9d-4408-a1cf-b6bbdf643adc.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69543-375-10 | 69543037510 | 100 CAPSULE in 1 BOTTLE (69543-375-10) | 100 capsule | 2016-07-13 | 0000-00-00 | No | No | Current |