Bupropion Hydrochloride
- Product NDC
- 68788-7793
- 11-digit product format
- 687887793
- Labeler code
- 68788
- Product ID
- 68788-7793_fe9c69c0-3a09-4dbe-b79f-f695468cbd1b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA205794
- Marketing category
- ANDA
- Marketing start
- 2020-10-13
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 200 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Bupropion Hydrochloride
- Brand name suffix
- SR
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BUPROPION HYDROCHLORIDE | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | ZG7E5POY8O |
| Rxcui | 993536 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68788-7793-1 | Bupropion HydrochlorideSR | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED, EXTENDED RE | 100 | | 7 |
| 68788-7793-2 | Bupropion HydrochlorideSR | 20 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED, EXTENDED RE | 20 | | 7 |
| 68788-7793-3 | Bupropion HydrochlorideSR | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED, EXTENDED RE | 30 | | 7 |
| 68788-7793-6 | Bupropion HydrochlorideSR | 60 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED, EXTENDED RE | 60 | | 7 |
| 68788-7793-8 | Bupropion HydrochlorideSR | 120 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED, EXTENDED RE | 120 | | 7 |
| 68788-7793-9 | Bupropion HydrochlorideSR | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED, EXTENDED RE | 90 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-7793 | BUPROPION HYDROCHLORIDE SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [PREFERRED PHARMACEUTICALS, INC.] | 5 | Current NDC, Legacy NDC, 6 package rows | 20250112_c0445fea-108f-4e00-a2ae-ebbdf2719947.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7793-1 | 68788779301 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-1) | 2020-10-13 | 0000-00-00 | No | No | Current |
| 68788-7793-2 | 68788779302 | 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-2) | 2020-10-13 | 0000-00-00 | No | No | Current |
| 68788-7793-3 | 68788779303 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-3) | 2020-10-13 | 0000-00-00 | No | No | Current |
| 68788-7793-6 | 68788779306 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-6) | 2020-10-13 | 0000-00-00 | No | No | Current |
| 68788-7793-8 | 68788779308 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-8) | 2020-10-13 | 0000-00-00 | No | No | Current |
| 68788-7793-9 | 68788779309 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-9) | 2020-10-13 | 0000-00-00 | No | No | Current |