ALEROFF
- Product NDC
- 81701-111
- 11-digit product format
- 817010111
- Labeler code
- 81701
- Product ID
- 81701-111_be4d907f-13cb-93a6-e053-2995a90af8b9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- HISTAMINE
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- OKSALUD COLOMBIA S A S
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2021-03-01
- Marketing end
- 0000-00-00
- Substance
- HISTAMINE
- Active strength
- 7 g/7mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 81701-111-01 | ALEROFF | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81701-111 | ALEROFF (HISTAMINE) LIQUID [OKSALUD COLOMBIA S A S] | 1 | Legacy NDC, 1 package rows | 20210326_be4d907f-13ca-93a6-e053-2995a90af8b9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81701-111-01 | 81701011101 | 30 mL in 1 BOTTLE, DROPPER (81701-111-01) | 30 ml | 2021-03-01 | 0000-00-00 | No | No | Current |