levocetirizine dihydrochloride
- Product NDC
- 68071-2836
- 11-digit product format
- 680712836
- Labeler code
- 68071
- Product ID
- 68071-2836_ef55e245-a756-67e2-e053-2995a90a4ef3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levocetirizine dihydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA210914
- Marketing category
- ANDA
- Marketing start
- 2019-04-01
- Marketing end
- 0000-00-00
- Substance
- LEVOCETIRIZINE DIHYDROCHLORIDE
- Active strength
- 3 mg/5mL
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [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 |
|---|
| 68071-2836-8 | levocetirizine dihydrochloride | 148 mL in 1 BOTTLE | SOLUTION | 148 | | 1 |
| 68071-2836-8 | levocetirizine dihydrochloride | 1 in 1 CARTON | SOLUTION | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2836 | LEVOCETIRIZINE DIHYDROCHLORIDE SOLUTION [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC, 2 package rows | 20221209_ef55e23c-731a-341c-e053-2995a90a0bf3.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 |
|---|
| 68071-2836-8 | 68071283608 | 1 BOTTLE in 1 CARTON (68071-2836-8) > 148 mL in 1 BOTTLE | 1 bottle | 2022-12-08 | 0000-00-00 | No | No | Current |