METFORMIN HYDROCHLORIDE
- Product NDC
- 71717-106
- 11-digit product format
- 717170106
- Labeler code
- 71717
- Product ID
- 71717-106_6e7926ae-f593-6fc6-e053-2991aa0af877
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Megalith Pharmaceuticals Inc
- Application
- ANDA205096
- Marketing category
- ANDA
- Marketing start
- 2017-12-18
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71717-106-11 | METFORMIN HYDROCHLORIDE | 1000 in 1 BOTTLE | TABLET, COATED | 1000 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71717-106 | METFORMIN HYDROCHLORIDE TABLET, COATED [MEGALITH PHARMACEUTICALS INC] | 3 | Legacy NDC, 1 package rows | 20180615_60643f78-fe80-8ee0-e053-2991aa0af3c1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 71717-106-11 | 71717010611 | 1000 in 1 BOTTLE | Historical |