OPIUM
- Product NDC
- 10191-1082
- 11-digit product format
- 101911082
- Labeler code
- 10191
- Product ID
- 10191-1082_19eb9717-94a1-2fd5-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Raw Opium Gum
- Dosage form
- PELLET
- Route
- SUBLINGUAL
- Labeler
- Remedy Makers
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-07-06
- Marketing end
- 0000-00-00
- Substance
- OPIUM
- Active strength
- 6 [hp_X]/1
- DEA schedule
- CII
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 10191-1082-2 | OPIUM | 160 in 1 VIAL, GLASS | PELLET | 160 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10191-1082 | OPIUM (RAW OPIUM GUM) PELLET [REMEDY MAKERS] | 2 | Legacy NDC, 1 package rows | 20230309_19eb9717-94a0-2fd5-e054-00144ff8d46c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10191-1082-2 | 10191108202 | 160 in 1 VIAL, GLASS | Historical |