Progesterone
- Product NDC
- 68071-2770
- 11-digit product format
- 680712770
- Labeler code
- 68071
- Product ID
- 68071-2770_e3dab203-488e-af9d-e053-2995a90a3043
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Progesterone
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA205229
- Marketing category
- ANDA
- Marketing start
- 2021-04-12
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-2770-9 | Progesterone | 90 in 1 BOTTLE | CAPSULE | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2770 | PROGESTERONE CAPSULE [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC, 1 package rows | 20220717_e3dab203-488d-af9d-e053-2995a90a3043.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 |
|---|
| 68071-2770-9 | 68071277009 | 90 CAPSULE in 1 BOTTLE (68071-2770-9) | 90 capsule | 2022-07-15 | 0000-00-00 | No | No | Current |