OPIUM
- Product NDC
- 10191-1089
- 11-digit product format
- 101911089
- Labeler code
- 10191
- Product ID
- 10191-1089_1a7658ae-18ff-0bca-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Raw Opium Gum
- Dosage form
- PELLET
- Route
- SUBLINGUAL
- Labeler
- Remedy Makers
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-07-09
- Marketing end
- 0000-00-00
- Substance
- OPIUM
- Active strength
- 6 [hp_C]/1
- DEA schedule
- CII
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 10191-1089 | I | Inactivated by FDA | 2026-07-31 | ||
| excluded package | package | 10191-1089 | 10191-1089-2 | I | Inactivated by FDA | 2026-07-31 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 10191-1089-2 | 2025-01-30 | C162847 | 48780-1 | 9d75b9d0-c9c4-f424-e053-dadaa90a57ce | 1a7658ae-18fe-0bca-e054-00144ff88e88 |
| 10191-1089-2 | 2023-03-07 | C162847 | 48780-1 | 9d75b9d0-c9c4-f424-e053-dadaa90a57ce | 1a7658ae-18fe-0bca-e054-00144ff88e88 |
| 10191-1089-2 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-c9c4-f424-e053-dadaa90a57ce | 1a7658ae-18fe-0bca-e054-00144ff88e88 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10191-1089-2 | OPIUM | 166 in 1 VIAL, GLASS | PELLET | 166 | 2 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| OPIUM | ACTIVE INGREDIENT | 37M3MZ001L | OPIUM (RAW OPIUM GUM) PELLET [REMEDY MAKERS] | 1 | |
| OPIUM | ACTIVE MOIETY | 37M3MZ001L | OPIUM (RAW OPIUM GUM) PELLET [REMEDY MAKERS] | 1 | |
| LACTOSE | INACTIVE INGREDIENT | J2B2A4N98G | OPIUM (RAW OPIUM GUM) PELLET [REMEDY MAKERS] | 1 | |
| SUCROSE | INACTIVE INGREDIENT | C151H8M554 | OPIUM (RAW OPIUM GUM) PELLET [REMEDY MAKERS] | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 10191-1089 | OPIUM (RAW OPIUM GUM) PELLET [REMEDY MAKERS] | 2 | Legacy NDC, 1 package rows | 20230309_1a7658ae-18fe-0bca-e054-00144ff88e88.zip |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 10191-1089-2 | 10191108902 | 166 in 1 VIAL, GLASS | Historical |