Progesterone
- Product NDC
- 71205-684
- 11-digit product format
- 712050684
- Labeler code
- 71205
- Product ID
- 71205-684_e1546b35-cfa8-4808-9652-db1ba675a4e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Progesterone
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA205229
- Marketing category
- ANDA
- Marketing start
- 2021-01-08
- Substance
- PROGESTERONE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Progesterone [CS], Progesterone [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 4G7DS2Q64Y | PROGESTERONE | 57-83-0 | PROGESTERONE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-684-30 | 71205068430 | 30 CAPSULE in 1 BOTTLE (71205-684-30) | 30 capsule | 2022-08-11 | No | No | Historical |
| 71205-684-60 | 71205068460 | 60 CAPSULE in 1 BOTTLE (71205-684-60) | 60 capsule | 2022-08-11 | No | No | Historical |
| 71205-684-90 | 71205068490 | 90 CAPSULE in 1 BOTTLE (71205-684-90) | 90 capsule | 2022-08-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Progesterone Capsules | Proficient Rx LP | 2022-08-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |