PROGESTERONE
- Product NDC
- 69452-149
- 11-digit product format
- 694520149
- Labeler code
- 69452
- Product ID
- 69452-149_73113fdd-1ff9-419e-8c29-3e82c8898cce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PROGESTERONE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bionpharma Inc.
- Application
- ANDA200900
- Marketing category
- ANDA
- Marketing start
- 2016-09-20
- Substance
- PROGESTERONE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Progesterone [CS], Progesterone [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PROGESTERONE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PROGESTERONE | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4G7DS2Q64Y |
| Rxcui | 260243, 312641 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69452-149-20 | PROGESTERONE | 100 in 1 BOTTLE | CAPSULE | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69452-149 | PROGESTERONE CAPSULE [BIONPHARMA INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20180413_3acad9b0-7ec6-4d5e-9852-32ffadbbed6d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69452-149-20 | 69452014920 | 100 CAPSULE in 1 BOTTLE (69452-149-20) | 100 capsule | 2016-09-20 | 0000-00-00 | No | No | Current |