NAFASOLINA
- Product NDC
- 48462-001
- 11-digit product format
- 484620001
- Labeler code
- 48462
- Product ID
- 48462-001_baf40d48-157a-8c07-e053-2a95a90a2c28
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- NAPHAZOLINE HYDROCHLORIDE
- Dosage form
- SOLUTION/ DROPS
- Route
- NASAL
- Labeler
- DUY DRUGS, INC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-02-15
- Marketing end
- 0000-00-00
- Substance
- NAPHAZOLINE HYDROCHLORIDE
- Active strength
- 0 mg/100mg
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 48462-001-01 | NAFASOLINA | 13310 mg in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 13310 | | 1 |
| 48462-001-02 | NAFASOLINA | 13310 in 1 CARTON | SOLUTION/ DROPS | 13310 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48462-001 | NAFASOLINA (NAPHAZOLINE HYDROCHLORIDE) SOLUTION/ DROPS [DUY DRUGS, INC] | 1 | Legacy NDC, 2 package rows | 20210215_baf40abf-9623-e80f-e053-2a95a90ae9cd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48462-001-01 | 48462000101 | 13310 mg in 1 BOTTLE, DROPPER | 13310 mg | | | | | Historical |
| 48462-001-02 | 48462000102 | 13310 BOTTLE, DROPPER in 1 CARTON (48462-001-02) > 13310 mg in 1 BOTTLE, DROPPER (48462-001-01) | | 2021-02-15 | 0000-00-00 | No | No | Current |