Bupropion Hydrochloride
- Product NDC
- 72162-2098
- 11-digit product format
- 721622098
- Labeler code
- 72162
- Product ID
- 72162-2098_c9f7a97c-ab97-42a1-b768-dfaa4de4dd74
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076143
- Marketing category
- ANDA
- Marketing start
- 2006-01-17
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 75 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 | 75 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | ZG7E5POY8O |
| Rxcui | 993691 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2098-1 | Bupropion Hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 104 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2098 | BUPROPION HYDROCHLORIDE TABLET, FILM COATED [BRYANT RANCH PREPACK] | 103 | Current NDC, 1 package rows | 20240830_f566f8b5-b3c1-4234-88bd-59a7b8dc801a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2098-1 | 72162209801 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-2098-1) | 2006-01-17 | No | No | Historical |