PROGESTERONE
- Product NDC
- 82804-268
- 11-digit product format
- 828040268
- Labeler code
- 82804
- Product ID
- 82804-268_199c8575-e113-468f-8eb7-c4930030649c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PROGESTERONE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA200900
- Marketing category
- ANDA
- Marketing start
- 2018-11-28
- Substance
- PROGESTERONE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Progesterone [CS], Progesterone [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PROGESTERONE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PROGESTERONE | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4G7DS2Q64Y |
| Rxcui | 312641 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82804-268-30 | PROGESTERONE | 30 in 1 BOTTLE | CAPSULE | 30 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-268-30 | 82804026830 | 30 CAPSULE in 1 BOTTLE (82804-268-30) | 30 capsule | 2026-02-19 | No | No | Current |