Midazolam Hydrochloride
- Product NDC
- 72162-1109
- 11-digit product format
- 721621109
- Labeler code
- 72162
- Product ID
- 72162-1109_f9324142-58b0-448d-b37d-f0f7025d02c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Midazolam Hydrochloride
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076379
- Marketing category
- ANDA
- Marketing start
- 2005-05-02
- Substance
- MIDAZOLAM HYDROCHLORIDE
- Active strength
- 2 mg/mL
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Midazolam Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MIDAZOLAM HYDROCHLORIDE | 2 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W7TTW573JJ |
| Rxcui | 422410 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1109-2 | Midazolam Hydrochloride | 1 in 1 CARTON | SYRUP | 1 | | 100 |
| 72162-1109-2 | Midazolam Hydrochloride | 118 mL in 1 BOTTLE, GLASS | SYRUP | 118 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1109 | MIDAZOLAM HYDROCHLORIDE SYRUP [BRYANT RANCH PREPACK] | 100 | Current NDC, 2 package rows | 20231026_1a701d59-3a30-4a4b-a5dd-51f01ba9c5cc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1109-2 | 72162110902 | 1 BOTTLE, GLASS in 1 CARTON (72162-1109-2) / 118 mL in 1 BOTTLE, GLASS | 2023-10-25 | No | No | Current |