SPIRONOLACTONE
- Product NDC
- 16714-085
- 11-digit product format
- 167140085
- Labeler code
- 16714
- Product ID
- 16714-085_192faced-01bc-42a8-ad1f-492d6c3108f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SPIRONOLACTONE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NorthStar Rx LLC
- Application
- ANDA089424
- Marketing category
- ANDA
- Marketing start
- 2020-04-23
- Marketing end
- 0000-00-00
- Substance
- SPIRONOLACTONE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 16714-085 | SPIRONOLACTONE TABLET SPIRONOLACTONE TABLET, FILM COATED [NORTHSTAR RX LLC] | 5 | Legacy NDC | 20240802_2aead427-3e25-4a87-a858-f2bd7642baf5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-085-01 | 16714008501 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16714-085-01) | 2020-04-23 | 0000-00-00 | No | No | Current |
| 16714-085-02 | 16714008502 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16714-085-02) | 2020-04-23 | 0000-00-00 | No | No | Current |