Progesterone
- Product NDC
- 76420-071
- 11-digit product format
- 764200071
- Labeler code
- 76420
- Product ID
- 76420-071_9a710009-a90f-095c-e053-2a95a90a1857
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Progesterone
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- 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
- 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 |
|---|
| 76420-071-10 | 76420007110 | 100 CAPSULE in 1 BOTTLE, PLASTIC (76420-071-10) | 100 capsule | 2019-12-24 | 0000-00-00 | No | No | Current |
| 76420-071-30 | 76420007130 | 30 CAPSULE in 1 BOTTLE, PLASTIC (76420-071-30) | 30 capsule | 2019-12-24 | 0000-00-00 | No | No | Current |
| 76420-071-90 | 76420007190 | 90 CAPSULE in 1 BOTTLE, PLASTIC (76420-071-90) | 90 capsule | 2019-12-24 | 0000-00-00 | No | No | Current |