OPIUM
- Product NDC
- 10191-1093
- 11-digit product format
- 101911093
- Labeler code
- 10191
- Product ID
- 10191-1093_c01f3bdf-9010-4318-9513-a9eeedbaf260
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- RAW OPIUM GUM
- Dosage form
- PELLET
- Route
- SUBLINGUAL
- Labeler
- Remedy Makers
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2001-11-21
- Marketing end
- 0000-00-00
- Substance
- OPIUM
- Active strength
- 30 [hp_C]/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 |
|---|
| 10191-1093-2 | OPIUM | 137 in 1 VIAL, GLASS | PELLET | 137 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10191-1093 | OPIUM (RAW OPIUM GUM) PELLET [REMEDY MAKERS] | 2 | Legacy NDC, 1 package rows | 20110309_409cda28-3869-497e-ad20-a30499a74bd0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10191-1093-2 | 10191109302 | 137 in 1 VIAL, GLASS | Historical |