Progesterone
- Product NDC
- 71205-293
- 11-digit product format
- 712050293
- Labeler code
- 71205
- Product ID
- 71205-293_4e6c6c6c-0e4e-49a2-a344-cecf0eb86f75
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Progesterone
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA200456
- Marketing category
- ANDA
- Marketing start
- 2012-10-04
- 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 |
|---|
| 71205-293 | PROGESTERONE CAPSULE [PROFICIENT RX LP] | 3 | Legacy NDC | 20200313_ecaac22a-8efa-458a-81ac-962603b5fc91.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-293-30 | 71205029330 | 30 CAPSULE in 1 BOTTLE, PLASTIC (71205-293-30) | 30 capsule | 2019-07-01 | 0000-00-00 | No | No | Current |
| 71205-293-60 | 71205029360 | 60 CAPSULE in 1 BOTTLE, PLASTIC (71205-293-60) | 60 capsule | 2019-07-01 | 0000-00-00 | No | No | Current |
| 71205-293-90 | 71205029390 | 90 CAPSULE in 1 BOTTLE, PLASTIC (71205-293-90) | 90 capsule | 2019-07-01 | 0000-00-00 | No | No | Current |