Glyburide and Metformin Hydrochloride
- Product NDC
- 71335-0360
- 11-digit product format
- 713350360
- Labeler code
- 71335
- Product ID
- 71335-0360_070b40e6-7d48-4193-a3c5-2599e3e6dbaf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide and Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077870
- Marketing category
- ANDA
- Marketing start
- 2007-11-14
- Substance
- GLYBURIDE; METFORMIN HYDROCHLORIDE
- Active strength
- 5; 500 mg/1; mg/1
- Pharmacologic classes
- Biguanide [EPC], Biguanides [CS], Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Glyburide and Metformin Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GLYBURIDE | 5 mg/1 |
| METFORMIN HYDROCHLORIDE | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SX6K58TVWC, 786Z46389E |
| Rxcui | 861753 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-0360-1 | Glyburide and Metformin Hydrochloride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 105 |
| 71335-0360-3 | Glyburide and Metformin Hydrochloride | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 105 |
| 71335-0360-4 | Glyburide and Metformin Hydrochloride | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 105 |
| 71335-0360-5 | Glyburide and Metformin Hydrochloride | 120 in 1 BOTTLE | TABLET, FILM COATED | 120 | | 105 |
| 71335-0360-6 | Glyburide and Metformin Hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 105 |
| 71335-0360-7 | Glyburide and Metformin Hydrochloride | 180 in 1 BOTTLE | TABLET, FILM COATED | 180 | | 105 |
| 71335-0360-8 | Glyburide and Metformin Hydrochloride | 25 in 1 BOTTLE | TABLET, FILM COATED | 25 | | 105 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-0360 | GLYBURIDE AND METFORMIN HYDROCHLORIDE TABLET, FILM COATED [BRYANT RANCH PREPACK] | 105 | Current NDC, Legacy NDC, 7 package rows | 20240822_4dcef36f-000e-43f5-8d67-0e2a079ab2c6.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 |
|---|
| 71335-0360-1 | 71335036001 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0360-1) | 2018-06-08 | 0000-00-00 | No | No | Current |
| 71335-0360-3 | 71335036003 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0360-3) | 2018-03-16 | 0000-00-00 | No | No | Current |
| 71335-0360-4 | 71335036004 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0360-4) | 2018-10-29 | 0000-00-00 | No | No | Current |
| 71335-0360-5 | 71335036005 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0360-5) | 2024-05-29 | 0000-00-00 | No | No | Current |
| 71335-0360-6 | 71335036006 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0360-6) | 2018-02-26 | 0000-00-00 | No | No | Current |
| 71335-0360-7 | 71335036007 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-0360-7) | 2024-05-29 | 0000-00-00 | No | No | Current |
| 71335-0360-8 | 71335036008 | 25 TABLET, FILM COATED in 1 BOTTLE (71335-0360-8) | 2018-03-30 | 0000-00-00 | No | No | Current |