41163-351 : Equaline 150 mg Oral Tablet
NDC: | 41163-351 |
Labeler: | Supervalu Inc. |
Product Type: | Human OTC Drug |
Drug Name: | Equaline |
Dosage Form: | Oral Tablet |
Application #: | ANDA200536 |
Rev. Date: |
Appearance:
Markings: | 9R |
Shapes: |
Oval |
Colors: |
Pink |
Size (mm): | 12 |
Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. |
NDC Package Codes:
- 41163-351-24: 24 BLISTER PACK IN 1 CARTON (41163‑351‑24) > 1 TABLET IN 1 BLISTER PACK
- 41163-351-50: 1 BOTTLE IN 1 CARTON (41163‑351‑50) > 50 TABLET IN 1 BOTTLE
- 41163-351-65: 1 BOTTLE IN 1 CARTON (41163‑351‑65) > 65 TABLET IN 1 BOTTLE
Active Ingredients:
- Ranitidine Hydrochloride
Dosage Strength:
- 150 mg
Inactive Ingredients:
- Silicon Dioxide
- Croscarmellose Sodium
- Hypromelloses
- Ferric Oxide Red
- Magnesium Stearate
- Cellulose, Microcrystalline
- Polyethylene Glycols
- Talc
- Titanium Dioxide
Related Products:
Based on records with the same trade name.- 41163-163 Equaline .46 mg/100ml Topical Liquid by Supervalu Inc.
- 41163-177 Equaline .46 mg/100ml Topical Liquid by Supervalu Inc.
- 41163-258 Equaline 62 ml/100ml Topical Liquid by Supervalu Inc.
- 41163-259 Equaline 62 ml/100ml Topical Liquid by Supervalu Inc.
- 41163-358 Equaline 13 mg/ml Topical Lotion by Supervalu Inc.
- 41163-828 Equaline 20 mg/ml Topical Paste by Supervalu Inc.
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.