PROGESTERONE
- Product NDC
- 10888-7136
- 11-digit product format
- 108887136
- Labeler code
- 10888
- Product ID
- 10888-7136_cfbb9566-cfae-4fd3-8256-384521cefcf0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PROGESTERONE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Banner Pharmacaps
- Application
- ANDA200900
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- Marketing end
- 0000-00-00
- Substance
- PROGESTERONE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Progesterone [CS],Progesterone [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 10888-7136-2 | PROGESTERONE | 100 in 1 BOTTLE | CAPSULE | 100 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10888-7136 | PROGESTERONE CAPSULE [BANNER PHARMACAPS] | 11 | Legacy NDC, 1 package rows | 20140101_f7cc2093-86ad-4959-a4ed-7a72148f3d74.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10888-7136-2 | 10888713602 | 100 in 1 BOTTLE | Historical |