Miclara LQ
- Product NDC
- 70868-730
- 11-digit product format
- 708680730
- Labeler code
- 70868
- Product ID
- 70868-730_d67cfbdf-9636-4ba6-e053-2a95a90aacbb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TRIPROLIDINE HYDROCHLORIDE
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Key Therapeutics
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-05-15
- Marketing end
- 0000-00-00
- Substance
- TRIPROLIDINE HYDROCHLORIDE
- Active strength
- 1 mg/5mL
- 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 |
|---|
| 70868-730-16 | Miclara LQ | 473 mL in 1 BOTTLE | LIQUID | 473 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70868-730 | MICLARA LQ (TRIPROLIDINE HYDROCHLORIDE) LIQUID [KEY THERAPEUTICS] | 3 | Legacy NDC, 1 package rows | 20220205_b1e0f143-e192-4bab-9163-ae21c765b765.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 |
|---|
| 70868-730-16 | 70868073016 | 473 mL in 1 BOTTLE (70868-730-16) | 473 ml | 2020-05-15 | 0000-00-00 | No | No | Current |