bupropion Hydrochloride
- Product NDC
- 72162-2401
- 11-digit product format
- 721622401
- Labeler code
- 72162
- Product ID
- 72162-2401_2b800bb5-b906-42b0-bc63-164f62bd7db1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206975
- Marketing category
- ANDA
- Marketing start
- 2016-08-19
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- bupropion Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BUPROPION HYDROCHLORIDE | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | ZG7E5POY8O |
| Rxcui | 993687 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2401-1 | bupropion Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2401 | BUPROPION HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] | 101 | Current NDC, 1 package rows | 20250108_4971c3cb-07c4-4c65-a16a-f1700e523147.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2401-1 | 72162240101 | 100 TABLET in 1 BOTTLE (72162-2401-1) | 100 tablet | 2024-10-02 | No | No | Historical |