NDC 50845-0169-2 - ProBLEN Estrogen and Progesterone
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 50845-0169
- Requested NDC
- 50845-0169-2
- Package NDCs from labels
- 50845-0169-1, 50845-0169-2, 50845-0169-3
- Manufacturer
- Liddell Laboratories, Inc.
- Effective date
- 2012-02-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ProBLEN Estrogen and Progesterone | Liddell Laboratories, Inc. | 2012-02-06 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50845-0169-3 | 2019-11-13 | C162847 | 48780-1 | 97449f38-bab0-f6ea-e053-dbdaa90aa703 | ProBLEN Estrogen and Progesterone |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50845-0169-1 | ProBLEN Estrogen and Progesterone | 30 mL in 1 BOTTLE, SPRAY | SPRAY | 30 | 1 | |
| 50845-0169-2 | ProBLEN Estrogen and Progesterone | 1 in 1 CARTON | SPRAY | 1 | 1 | |
| 50845-0169-3 | ProBLEN Estrogen and Progesterone | 1 in 1 CARTON | SPRAY | 1 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50845-0169 | PROBLEN ESTROGEN AND PROGESTERONE (AGNUS CASTUS, ANGELICA SINENSIS, RADIX, APIS MELLIFICA, ARNICA MONTANA, CIMICIFUGA RACEMOSA, ESTRADIOL, ESTRIOL, FOLLICULINUM, GALIUM APARINE, GLYCYRRHIZA GLABRA, KOREAN GINSENG,) SPRAY [LIDDELL LABORATORIES, INC.] | 1 | Legacy NDC, 3 package rows | 20120207_02eff84a-7cf2-401d-914e-d84003f56760.zip |
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.