Metformin Hydrochloride
- Product NDC
- 64205-220
- 11-digit product format
- 642050220
- Labeler code
- 64205
- Product ID
- 64205-220_b701df7c-4e31-4228-ab81-87d8c13bc54a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ReadyMeds
- Application
- ANDA077880
- Marketing category
- ANDA
- Marketing start
- 2012-12-17
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 64205-220-60 | Metformin Hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | | 8 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64205-220 | METFORMIN HYDROCHLORIDE TABLET [READYMEDS] | 8 | Legacy NDC, 1 package rows | 20140630_9411b1e8-6715-4d62-9861-ccc052f65c8e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64205-220-60 | 64205022060 | 60 in 1 BOTTLE | Historical |